Abstract
The importance of food safety to public health is reflected in its inclusion in the United Nations Sustainable Development Goals (SDGs)—SDG 2 (Zero Hunger), SDG 3 (Good Health and Well-being), and SDG 12 (Responsible Consumption and Production)—and the World Health Organization’s food safety strategy. Its inclusion across multiple areas underscores how food safety is not an isolated objective but is closely tied to broader public health and sustainability goals. While the public often expects food to be “absolutely” safe, experts recognize that all foods carry a residual risk of causing foodborne illness and that zero risk is neither achievable nor desirable. Advances in diagnostics and surveillance systems (e.g., increases in test sensitivity and specificity) have increased the frequency of hazard detection in foods, including detection of hazards at levels that may pose minimal public health risks. However, efforts to manage these negligible risks can divert attention from more significant threats and may introduce unintended consequences that outweigh the intended benefits. To address this, holistic approaches and trade-off risk assessments are needed, accounting for the interrelationship between the health of humans, animals, and the environment (i.e., One Health) and evaluating both the costs and benefits of food safety measures, including direct expenses, externalities, social or legal constraints, and consumer preferences. Key tools enabling these risk assessments include Monte Carlo simulations and other modeling tools that are also being adopted for food safety applications, such as geographic information system models, agent-based models, and artificial intelligence (AI)-based predictive tools. These efforts can help define quantitative food safety goals that ensure appropriate, but not absolute, safety, so long as implemented controls are validated and verified. Technological advances, such as AI-enabled risk negotiation, offer new opportunities to integrate trade-offs in risk analysis and support more balanced, effective food safety strategies.
Key points
Zero risk of foodborne illness is neither achievable nor desirable; overly stringent food safety practices can lead to unintended consequences that outweigh their public health and societal benefits.
Better trade-off risk assessments and associated predictive and decision-making tools must be developed to support food safety decision-making.
Further development and implementation of risk negotiation approaches can help achieve societally acceptable sustainable food systems that produce sufficiently safe food.
Introduction
Food safety is a key determinant of public health (). According to the most current estimates by the World Health Organization (WHO), microbial foodborne pathogens cause 600 million cases of illness annually (). These illnesses result in 420,000 deaths ()—a third (125,000 deaths/year) in children aged under 5 years ()—and a loss of 33 million disability-adjusted life years (DALYs) (). In 2019, the World Bank estimated that foodborne diseases cost US$110 billion/year in productivity loss and medical costs in low- and middle-income countries alone (). The inclusion of food safety within the United Nations (UN) Sustainable Development Goals (SDGs) (), which are a part of the 2030 Agenda for Sustainable Development, underscores not only its global importance to public health but also its close interconnection with sustainability. Accordingly, the WHO Global Strategy for Food Safety 2022–2030 aims to reduce the burden of foodborne illness (), and the WHO is currently working with the World Bank to provide updated disease burden estimates ().
Various food production and processing strategies, such as good agricultural practices, drying, pasteurization, sanitary equipment design, refrigeration and freezing throughout distribution, and strict microbiological limits for foods, can help reduce the presence of microbial foodborne pathogens and improve food safety. However, many of these approaches come with unintended consequences that can affect and limit their application, ranging from increased food insecurity to a variety of negative environmental impacts, including increased food waste. In addition, some technologies carry high costs (e.g., for equipment, power, and labor) or logistical challenges (e.g., access to skilled labor or necessary maintenance) that hamper their implementation in many parts of the world. Hence, for some food safety approaches, mandated use or overly stringent requirements (e.g., with regard to microbiological testing) could negatively impact food availability and sustainability.
The essentially ubiquitous trade-offs associated with strategies to improve microbial food safety represent an often underappreciated and unaddressed challenge. More specifically, while some groups and individuals may desire food that is “completely” safe, absolute safety, even regarding a specific challenge such as microbial food safety, is neither possible nor desirable (). This problem has been acknowledged since at least 1993, when the Organisation for Economic Co-operation and Development defined safe food as “a reasonable certainty that no harm will result from intended uses under the anticipated conditions of consumption” (). Consequently, food safety decisions at all levels (governments, companies, and individuals) must weigh various trade-offs to determine what constitutes “sufficiently safe” food or what food can be considered to show “reasonable certainty that no harm will result from intended use” (). This approach of defining “sufficiently safe” food is also exemplified by concepts such as the “Appropriate Level of Protection” (ALOP) (, ), which involves defining acceptable levels of risk; this approach has been applied to set microbiological benchmarks for food safety (e.g., log reduction targets for foodborne pathogens). Another approach for defining acceptable levels of risk, particularly for food additives, includes setting a one-in-a-million risk level as “acceptable”, with the United States Food and Drug Administration (FDA) declaring that lifetime risks lower than this one-in-a-million level should be considered de minimis under the so-called Delaney Amendment (). However, the de minimis principle could be considered as an arbitrary threshold and thus may not be considered a satisfactory approach for distinguishing between negligible and non-negligible risk (). Similarly, defining what is an “appropriate” level of protection can be challenging. Hence, approaches and tools for improving and facilitating food safety decisions must be further developed and applied to better reach consensus on what constitutes acceptable or tolerable risks (), as well as negligible or non-negligible risks, for different foods across societies. Consistent with this, increasing the use of food chain information, scientific evidence, and risk assessment in making risk management decisions is a strategic pillar of the WHO Global Strategy for Food Safety ().
This article details how global food systems are increasingly facing more, and sometimes competing, demands, such as (i) supporting public health protection by ensuring food safety while also (ii) striving for sustainability in food systems (including reduction of food waste). For example, discarding any food that tests positive for foodborne pathogens, without considering the likelihood of the food causing foodborne illness, may help safeguard public health but also contributes to food waste and associated consequences (e.g., greenhouse gas emissions). Thus, due to the “interconnectedness” of our food system (as illustrated by the One Health concept), there is a need to optimize, balance, and negotiate strategies that can improve the safety and sustainability of food systems to provide well-being and health to global populations while protecting constituents of food systems (e.g., farmers and food businesses) and the planet (e.g., animals, plants, and the environment). These challenges bring new urgency to the prioritization of risk-based decision-making—which has been previously been detailed by various agencies and groups (, , ) and will be discussed later in this manuscript—over hazard-based decision-making, which could be described as primarily focusing on pathogen detection and elimination. This focus on risk-based decision-making needs to overcome implementation barriers (e.g., challenges in defining acceptable food safety risk levels) and move beyond current approaches, including ALOP and “As Low as Reasonably Achievable” (ALARA) (). Furthermore, explicit consideration of residual risk in policymaking will be essential to comprehensively drive implementation of risk-based food safety systems. The use of new approaches—e.g., artificial intelligence (AI) or new modeling tools—can help define acceptable levels of risk and consider residual risks while balancing competing interests in our complex food systems. While the focus of this article is on microbial food safety, many of the concepts detailed here, and particularly the need for trade-off risk assessments, also apply to chemical food safety risks, where some trade-off risk assessments have already been applied (e.g., ).
Microbial food safety in the context of human health, One Health, and food system sustainability
Human health impacts of foodborne microbial pathogens
Pathogens commonly associated with foodborne illness cases include the bacteria Salmonella, certain Escherichia coli strains, Listeria monocytogenes, and Campylobacter (), and viruses such as norovirus, hepatitis A virus, and hepatitis E virus (). While many of these pathogens (e.g., norovirus) typically cause mild foodborne illnesses, characterized by vomiting and diarrhea, several pathogens can cause more severe illnesses. For example, L. monocytogenes typically causes severe invasive infections with symptoms including septicemia, encephalitis, and miscarriage; approximately 90% of listeriosis infections result in hospitalization, and 20% cause death. For other pathogens, specific strains may have a propensity to cause more serious infections. Enterohemorrhagic E. coli (EHEC), for example, are a subgroup of E. coli that can cause particularly severe symptoms, including kidney failure and hemolytic uremic syndrome (). Other E. coli subtypes may either cause milder symptoms (e.g., diarrhea) or are not typically linked to foodborne disease at all (). In addition, susceptibility to foodborne infections can differ substantially between population subsegments, with young, elderly, and immunocompromised individuals often carrying a higher risk.
Foodborne pathogens can also cause long-term sequelae with substantial public health impacts. For example, Campylobacter can trigger Guillain-Barré syndrome, a neurological autoimmune disorder whose symptoms include muscle weakness and sometimes paralysis; estimates of its occurrence range from 21.5–172 cases per 100,000 Campylobacter cases (, ). Other long-term sequelae of Campylobacter, Salmonella, Shigella, and Yersinia infections can include reactive arthritis (–). In addition to direct public health impacts, microbial foodborne illnesses have many other indirect impacts, including contributions to malnutrition and poor infant health (e.g., due to reduced nutrient absorption in individuals with re-occurring foodborne illness episodes) ().
Microbial food safety and One Health
Many microbial food safety issues are closely linked to the microbial safety and quality of water and to animal health, as detailed in a number of reviews on One Health and food safety (e.g., , ). For example, contaminated water can be an important source of pathogen contamination of different foods at different stages of the food chain, including primary production (e.g., if contaminated water is used for irrigation of produce), food processing, and consumer food preparation. Food animals infected with or carrying foodborne pathogens (e.g., Salmonella) not only represent an important “direct” source of foodborne pathogens (e.g., through contaminated meat, milk, or eggs) but also contribute more indirectly to transmission and dispersal. For example, runoff from animal facilities can introduce foodborne pathogens into water sources used for irrigation () as well as directly into pre-harvest environments, such as produce fields. Although less well documented, airborne dispersal of foodborne pathogens from livestock operations may also contribute to contamination of pre-harvest environments (, ). Wildlife, too, has been found to lead to the dispersal of foodborne pathogens through contamination of water or direct fecal deposition into pre-harvest environments (including in foodborne disease outbreaks linked to contaminated produce) (, ). As microbial food safety can be considered a One Health issue (, ), strategies designed to reduce food safety risks are likely to have wide-ranging impacts—both positive and negative (see Figure 1 and Table 1 for examples of food safety interventions and associated trade-offs).
Figure 1
Table 1
| Food safety strategy/interventions | Potential negative impacts/unintended consequences | Details |
|---|---|---|
| Heat treatment (e.g., pasteurization), potentially with higher heats or extended times | Reduced nutritional content of foods, leading to reduced access to nutritious food and possibly increased risk of vitamin deficiencies | Heat treatment of fruit juices has been shown to reduce vitamin content (e.g., vitamin C) () |
| Chemical antimicrobials | Presence of chemical contaminants in foods that may impact human health, representing chemical food safety risks (e.g., increased risk of certain cancers) | Nitrites used to prevent the growth of Clostridium botulinum () in processed meat can lead to the formation of nitrosamines (, ). However, some research indicates that nitrates may positively impact cardiovascular health () |
| Chemical sanitation to reduce pathogens in food production (e.g., with peracetic acid) | Use of chemicals in food processing with possible negative impacts on worker welfare | Worker exposure to compounds (e.g., peracetic acid) that can be corrosive to eyes and skin () |
| Wildlife control and exclusion | Degradation of natural ecosystems and negative impacts on biodiversity | Excessive control of wildlife or removal of wildlife habitats to prevent pathogen introduction into pre-harvest environments may negatively impact biodiversity () |
| Overly conservative decisions to dispose of food products that (i) test positive for indicator organisms or (ii) were produced in food environments where index or indicator organisms were detected | Excessive food waste with associated negative environmental impacts and possibly reduced food availability | Detection of indicator organisms (e.g., coliforms), which have historically been used to characterize hygienic conditions, may be used inappropriately to classify a food as adulterated, leading to unnecessary product disposition and destruction () |
| “Environmentally unfriendly” packaging material (to reduce real or perceived food safety issues) | Excessive waste of materials used in food production and processing, leading to degradation of natural ecosystems (e.g., through increased microplastics pollution) | Consumer demand or other factors may lead to excessive use of packing materials to address perceived food safety risks that are minimal or unsupported. For example, despite limited evidence () that SARS-CoV-2 can be transmitted through consumption of contaminated food, a study () reported that 40% of surveyed consumers regarded COVID-19 concerns as very or extremely important in their decision to purchase food packaged in single-use plastics |
| Capital-intensive processing technologies and food safety strategies | Excessive food cost and resulting food security challenges if expensive microbial reduction processes are required | Use of high-pressure processing can enhance the safety of certain products but requires large investments into equipment, and hence, may increase food prices |
| Energy-intensive approaches that can decrease food safety risks (e.g., freezing or refrigeration) | Excessive energy use leading to increased emissions with associated negative environmental impacts | Guidance documents and regulations may require stringent practices that substantially increase energy consumption and business costs but provide minimal improvements in food safety over slightly less stringent practices. For example, slightly less cold frozen storage temperatures may substantially decrease costs and energy usage but are expected to have minimal food safety impacts |
| Excessive water usage to support pathogen control efforts (e.g., excessive cleaning and sanitation, frequent water changes in hydroponics) | Excessive water use, which can lead to water shortages and degradation of natural ecosystems | Water-intensive practices may be required by regulation or customer requirements to help create (sanitation) clean breaks (). For example, construction of a commercial-scale brewery was halted after protests about exacerbation of water scarcity () |
| Excessive testing of foods with highly sensitive methods that detect pathogen levels unlikely to cause human disease | Negative publicity (e.g., recalls of produce) that drives consumers to less safe and/or healthy food options | A study that assessed meat recalls over 20 years found that successive recall events cumulatively influence market patterns over longer periods, suggesting that recall events can have long-term impacts on consumer trust in specific foods () |
Examples of possible negative impacts and unintended consequences (e.g., on sustainability and food availability) of different food safety strategies and interventions.
Challenges for food system sustainability
Food safety is integral to UN SDG 2 (Zero Hunger), which aims to end hunger and achieve food security. This goal links to two further goals, SDG 3 (Good Health and Well-being) and SDG 12 (Responsible Consumption and Production), due to the need for safe and nutritious foods and the reduction of foodborne illness rates as well as the need for sustainable consumption and production patterns, which requires maintaining food safety while reducing food waste ().
Major challenges for sustainable food systems include (i) ensuring access to safe, abundant, and nutritious food, (ii) minimizing damage to natural ecosystems, and (iii) assuring quality of life and prosperity for individuals and communities associated with food production, processing, and distribution (). These major challenges must be addressed in the context of microbial food safety. Reducing public health impacts associated with microbial food safety is a significant challenge in its own, often classified as a “wicked problem” (, ), i.e., one that is challenging to address because of complex, contradictory, and changing requirements that are often difficult to recognize. “Wicked problems” have solutions that “are not true-or-false but better or worse” for which “the problem is never solved definitively” ().
Some key challenges associated with ensuring food safety include (i) diversity of the food supply (ranging from canned products to fresh meat, seafood, and produce), (ii) diversity of food production around the globe (from highly sophisticated production facilities to informal, and often unregulated, food establishments), (iii) foodborne pathogen contamination that can occur throughout the food value chain, including in agricultural environments, during harvesting, or in processing plants, retail establishments, restaurants, homes, and during various transportation steps, and (iv) the vast magnitude of food that must be produced. To illustrate the last point, in 2022, approximately 26.7 billion chickens were raised globally (), and the United States consumed approximately 6.2 billion pounds of tomatoes (). It is also worth noting that food production must continue to increase as the human population grows; it is estimated that the global food demand will increase by over 35% during the first half of the 21st century (i.e., from 2005, 2007, or 2010 through to 2050) (, ), exacerbating the challenges in building and maintaining sustainable and safe food systems.
Hazard- and risk-based approaches to microbial food safety
In the literature, it is not uncommon to see the mention of hazard- and risk-based approaches to food safety. Hazard-based approaches have been defined as approaches where the detection of a pathogen (typically a pathogenic species), regardless of level or other factors that impact risk, is used as a basis for legislation and/or risk management action (). Examples for this may be regulations that define any ready-to-eat (RTE) food that tests positive for L. monocytogenes as adulterated, regardless of levels or whether it would support growth of Listeria. Risk-based approaches, on the other hand, assess the probability of an adverse effect on an organism, including humans, given a certain exposure and scale risk mitigation strategies accordingly. The value of risk-based approaches to food safety is generally well recognized and broadly supported. For example, the WHO 2022–2030 Global Strategy for Food Safety recommends that “When setting and implementing regulatory requirements, the national food control systems should consider the whole food chain and take a risk-based approach” (). However, a delineation between hazard- and risk-based approaches to microbial food safety is not straightforward. Since zero risk is unattainable, i.e., some residual risk always remains despite food safety interventions (see Figure 2 for an example illustrating residual risk), even so-called hazard-based approaches typically involve decisions about acceptable risk, often defined indirectly through sensitivity of detection methods, sample sizes, and sampling frequency. For instance, a food safety system requiring RTE food to test negative for L. monocytogenes in a single 25 g sample accepts a higher level of risk than one requiring five 25 g samples (125 g total). In practice, food safety systems and approaches are thus probably better viewed as “hazard-focused” or “risk-focused”, as nearly all systems incorporate some degree of risk-based decision-making.
Figure 2
Development and implementation of risk-focused food safety approaches often utilize quantitative microbial risk assessment (QMRA) (as detailed further below). However, other and simpler alternative approaches (e.g., risk profiling) can also be utilized (); such alternative approaches to a full QMRA can be particularly important, as a frequently cited global challenge in implementing risk-based approaches is the availability of sufficient data and the capacity to collect and analyze it. However, some studies have also illustrated that meaningful QMRAs can be conducted with limited data, such as a recent QMRA of food safety interventions for Campylobacter spp. and Salmonella spp. along the chicken meat supply chain in Burkina Faso and Ethiopia ().
Definition of an acceptable risk (or an acceptable risk reduction), particularly for risk-focused food safety approaches, is important for establishing action levels [e.g., <x colony-forming unit (CFU) of a given pathogen in a certain food product]. However, as the term “acceptable risk” implies that some level of foodborne illness is acceptable, other terms such as “tolerable risk” or “achievable risk” may be preferable, as outlined in a report on risk assessments for waterborne diseases (). This report () also describes previous efforts to define acceptable microbial risks for water and thus may provide valuable learnings for food safety. Regarding food safety, previous attempts to help define acceptable risks included efforts to define ALOPs for different food safety hazards (e.g., L. monocytogenes), which could then be used to define specific food safety objectives (, ). However, the concept of ALOP and the associated nomenclature and definitions appear to have seen only limited global uptake since the World Trade Organization first described this concept in 1995 (). To address the issue of defining limits for presence and levels of foodborne pathogens, the concept of ALARA is sometimes used (); this approach, however, tends to focus more on technologically attainable risk reduction rather than societally acceptable risk levels and thus may be less valuable in the further development of risk-based food safety systems that consider societal costs, benefits, and trade-offs.
The choice of hazard- versus risk-focused food safety approaches can have important implications beyond the determination of regulatory limits for foodborne pathogens. For example, hazard-focused systems often emphasize end-product testing as a means of ensuring safety despite well-established evidence that it is largely ineffective at detecting contamination, especially when present at a low prevalence (), though it remains useful as a verification tool. Risk-focused approaches, on the other hand, facilitate the setting of performance criteria (PC), which specify goals for the effectiveness of food safety interventions, ideally throughout production and processing (, ). For example, risk-focused approaches may determine that a 5-log reduction in a target organism (e.g., the most heat-resistant vegetative pathogen in raw milk) may be sufficient for one product, whereas a 4-log reduction may suffice for another (e.g., Salmonella in almonds) (, ). While decisions on appropriate PC rely on assumptions about pathogen distribution and initial contamination concentration in raw materials, which should be verified (see Figure 3), decisions on specific PC (and whether they are “fit for purpose”) should also take into account an acceptable risk (e.g., x human illness cases per year), a consideration used when proposing that a 4-log reduction may be appropriate for Salmonella in almonds.
Figure 3
In contrast, hazard-focused approaches may aim to eliminate pathogens in finished products and even in areas of food processing facilities that pose minimal risk to the product (this approach could manifest by regulators not accounting for sampling areas when reviewing industry environmental sampling data). This can misdirect resources: as a somewhat extreme example, food business operators may allocate similar resources to address pathogen contamination in a zone 4 site (far from food contact surfaces) as to contamination in a zone 2 site (near exposed food), despite the much higher risk posed by the latter (). Similarly, a hazard-focused approach may give equal resources to control L. monocytogenes in products that do and do not support the growth of the organism, with the former representing a higher public health risk. These examples illustrate how a hazard-focused approach that demands equal attention be given to all hazards ignores the concept of opportunity cost, which Frank and Bernanke defined for an activity as “the value of the next best alternative that must be forgone to undertake the activity” (). In our specific scenario, the opportunity cost is the cost of improving pathogen control in zone 4 by redirecting resources to control the pathogen in zone 2, resulting in greater benefits for public health and food safety. Although opportunity costs are rarely formally analyzed in food safety, they likely influence food business decisions (). Consequently, a better understanding of these trade-offs could lead to more effective system design. Additionally, hazard-focused systems targeting zero detection may create other unintended consequences, such as less rigorous environmental sampling (e.g., sampling mostly clean surfaces), ultimately weakening validation and verification efforts.
Risk metrics
While risk-focused food safety approaches are frequently applied in public health decision-making, a somewhat “hidden” aspect of risk assessments is the variety of different metrics available to assess risk. These include different numerators, such as the number of foodborne illness cases, deaths, or quality-adjusted life years (QALYs), and different denominators, such as per serving, or per population per year (e.g., per million people per year) (see Figure 4 and Table 2 for further details on risk metrics, including QALYs). Crucially, the choice of risk metric may impact management decisions. For example, assessments using the number of foodborne illness cases in the United States may prioritize managing norovirus (estimated 5,461,731 cases and 149 deaths annually) () over L. monocytogenes (estimated 1,591 cases and 255 deaths annually), whereas assessments based on deaths would suggest the opposite; DALYs and QALYs represent one approach for unified risk metrics that take different dimensions of illness into account. Similarly, the choice of denominator can shape conclusions on food safety priorities. For example, based on “risk per serving”, raw milk has a substantially higher risk of causing foodborne illness than pasteurized milk. However, pasteurized milk represents a larger “risk per population” (as compared to raw milk) due to its far greater consumption (), suggesting that risk reduction efforts focusing on pasteurized products are justified even if raw milk represents a larger per serving risk. A published QMRA of Salmonella in almonds illustrates how risk metrics can guide food safety decisions. This analysis supported the use of a heat treatment process giving a 4-log reduction in this pathogen, which was estimated to result in fewer than one case of salmonellosis per year in the United States ().
Figure 4
Table 2
| Metrics | Description |
|---|---|
| Public health risk metrics: numerators1 | |
| Foodborne illness cases and deaths | Number of foodborne illness cases or deaths caused by a given pathogen |
| Disability-adjusted life year (DALY) | DALYs are used to quantify the number of years that are lost due to disability and premature death caused by a hazard (e.g., foodborne pathogen). DALYs involve the use of disability weights to quantify the severity of a health outcome, with 0 representing full health and 1 representing death ( |
| Quality-adjusted life year (QALY) | QALYs represent a measure that accounts for the years of life that are lived and the utility of those years, while accounting for the presence and severity of a health outcome due to a hazard (e.g., foodborne pathogen). QALYs involve the use of utility weights to calculate the utility loss associated with a health outcome, with 0 representing death and 1 representing full health ( |
| Food business risk metrics: numerators | |
| Cost of recall | Factors considered when determining the cost of a recall ( • direct costs such as (i) product destruction, (ii) plant shut down, and (iii) restarting product lines or a facility after recall; • indirect costs such as (i) loss of consumer trust and (ii) loss in the valuation of a food business. The annualized cost of a recall could be estimated by accounting for: • prevalence of a contaminated product • likelihood of a positive product test • likelihood of a product being tested (e.g., by regulatory agencies) |
| Cost of outbreak | Past studies considering the cost of outbreaks focused on the cost to: • business ( • consumers (e.g., cost of illness) • society (e.g., due to loss of productivity or use of public resources in the regulatory response to the outbreak) ( To assess the annualized cost of an outbreak, the likelihood of an outbreak needs to be quantified using an appropriate risk assessment that may define an outbreak as two (or more) reported disease cases that can be linked to a given product or facility (e.g., by whole genome sequencing) |
| Public health risk metrics: denominators | |
| Per serving | Number of foodborne illnesses or deaths expected across a certain number (e.g., 100,000) of servings, which can be calculated by accounting for the: • prevalence of contaminated servings • likelihood of illness due to exposure to a contaminated serving ( |
| Per population per year | Number of foodborne illnesses or deaths expected in a population over a year, obtained by incorporating: • risk per serving (see above) • annual amount of consumption (e.g., servings) across a population ( |
| Food business risk metrics: denominators | |
| Per number of products produced | The cost of recalls or outbreaks can be expressed per number of products produced or sold in a given year (for example, per number of servings or packages sold). This denominator would allow a food business to identify specific products or product lines that represent a higher risk |
| Per facility per year | The cost of recalls or outbreaks can be expressed per facility by accounting for products produced annually in a facility, as well as facility-specific factors that impact recall or outbreaks risks (e.g., the frequency and location of environmentally positive pathogen tests or the regulatory environment, which may affect the number of finished product tests performed by regulatory agencies; in some countries, virtually no finished product testing may be performed) |
Examples of different food safety risk metrics used in public health and by food businesses.
1While these public health risk metrics are typically used as numerators in food safety risk assessments, they can also be used as denominators. For example, cost-utility analyses use a ratio of the cost of an intervention as a numerator and QALYs as a denominator (
Importantly, risk-based decision-making at the food business level must often account for both public health risks and food business-level financial risks—sometimes out of necessity due to legal requirements such as the Sarbanes-Oxley Act in the United States (https://sarbanes-oxley-act.com/). Examples of food business-level risk metrics may include (i) recall risk and annualized recall cost, which factors in both the likelihood and financial impact of recalls, (ii) outbreak risk and associated annualized outbreak costs, considering the likelihood and financial impact of outbreaks, and (iii) costs of contamination events that do not lead to outbreaks or recalls, such as expenses related to product disposal, rework, or downgrading. The financial impacts of recalls and outbreaks should also account for the impacts of reputational damage.
As with public health metrics, different denominators may be used for business risk metrics, such as cost per unit produced or per facility. Since companies must prioritize addressing various types of risk, such as food safety, cybersecurity, or workplace safety, metrics that quantify the costs of different food safety risk management options can support more rational, data-driven decision-making. This applies both at the food business level and more broadly, for example when trade groups propose or mandate specific food safety practices. Financial risk metrics can also inform policy and regulatory decisions by identifying the most cost-effective risk management strategies. For instance, Ssemanda et al. (
Regulatory agency use of hazard- and risk-focused approaches
Regulatory agencies worldwide generally employ a combination of hazard- and risk-focused approaches to ensure food safety. Hazard-focused approaches are often favored for pathogens that cause severe illness, such as L. monocytogenes, and typically involve regulations that deem any detection of a pathogen in a finished product as evidence that a product is “unsafe” and, hence, adulterated. The current FDA policy on L. monocytogenes in RTE foods is widely regarded as an example of a hazard-focused approach (
Regulatory agencies may also use hazard- or risk-focused approaches beyond standard-setting, such as for prioritizing inspections and other regulatory actions (
Industry use of hazard- and risk-focused approaches
While regulatory agencies and international bodies, such as the Food and Agriculture Organization of the United Nations (FAO), frequently use QMRAs to guide food safety regulations and enforcement, food business operators (and particularly smaller food businesses) may often have limited access to such tools and resources. Food business operators with limited risk assessment expertise may also be prone to utilizing hazard-focused approaches and general food safety plans outlined in guidance documents (
While many companies implement fairly effective food safety systems using current practices, there are substantial opportunities to improve decision-making. Specifically, there is a need for (i) better and easier-to-use modeling and risk assessment tools suitable for industry and (ii) training and support for development and application of risk assessments; this is particularly important as regulators increasingly expect food safety systems to be “science- and risk-based”. Building science-based systems will, however, require consensus on clear goals regarding foodborne illness risk, defined using either (i) absolute targets (e.g., a maximum allowable probability of illness per serving of a product), (ii) relative targets (e.g., a specific percentage reduction in illness risk for a product or pathogen), or (iii) business risk-focused targets using financial or operational risk metrics. Scientific methods, such as risk assessments, can then be used to identify and evaluate the best strategies for achieving these goals.
Risk assessment and predictive modeling for food safety and sustainability
Modeling tools and quantitative risk assessments play a key role in developing systems that assure a level of food safety appropriate for a society or business, which by necessity must balance multiple objectives, including food safety, public health, and the sustainability of food and agricultural systems. Over the past few decades, numerous studies have developed food safety risk assessments. These assessments are valuable for setting priorities and standards, including by regulatory agencies. For example, a 2003 USDA/FDA risk-ranking report (
Monte Carlo simulation-based quantitative microbial risk assessments
Monte Carlo simulation-based quantitative microbial risk assessments (MC-QMRAs) were first applied to microbial food safety questions in the early 1990s (
An MC-QMRA (see Figure 5 for details) consists of two components: (i) a QMRA, which typically estimates the likelihood of adverse health outcomes from exposure to a hazard (e.g., a foodborne pathogen) and (ii) a Monte Carlo simulation, which quantifies variability and uncertainty in the model outcomes. A typical QMRA includes four stages: hazard identification, exposure assessment, dose–response characterization, and risk characterization (Figure 5) (
Figure 5

Conceptual framework for quantitative microbial risk assessment and Monte Carlo simulation and their integration for quantitative food safety risk assessments considering the various stages and perturbations in a food value chain. Integration of this framework into a more holistic approach to food safety decision-making is shown in Figure 6.
Within QMRAs, food value chain stages are typically represented using quantitative values or distributions that describe pathogen prevalence/concentration and/or process parameters (e.g., log reduction from heat treatment). Model inputs reflect either variability (natural heterogeneity within a system) and/or uncertainty (lack of knowledge or data) (
Monte Carlo simulations work by iteratively sampling from the defined distributions to generate a range of possible outcomes. A single iteration yields one estimate of a risk metric (e.g., illness risk per 100,000 servings), while many iterations (e.g., 100,000) generate a distribution of the risk metric. This allows estimation of the mean, range, and confidence intervals of risk that can be compared to real-world data on foodborne illness prevalence (if such data are available for a given food–pathogen combination) to gauge the accuracy of the risk estimates. In a second-order MC-QMRA, variability and uncertainty are modeled separately, which helps identify both the likely magnitude of risk and the areas needing improved data (
In addition to their use for risk rankings, MC-QMRAs are commonly used to evaluate potential regulatory interventions. Examples include (i) modeling of Salmonella transmission through eggs, which informed United States regulations mandating refrigeration (
Some MC-QMRAs were also specifically developed to support decision-making by industry, which often must manage microbial risks more stringently than required by regulation. For example, Zoellner et al. (
Other modeling tools used for microbial risk assessment and risk management
In addition to Monte Carlo simulations, other modeling tools are also being adopted for food safety applications, including geographic information system (GIS) models, agent-based models (ABMs), and AI-based predictive tools. Mechanistic models grounded in molecular biology are also emerging to help predict microbial inactivation (
GIS-based models
GIS-based models have diverse applications in food safety and can predict pathogen contamination risks based on spatial and environmental data. These models typically involve mapping locations of pathogen-positive sites and interpolating these data across geographical regions to identify high-risk areas and environmental drivers for pathogen contamination. Considered risk factors often vary spatially (e.g., proximity to pastures, roads, or water sources) and temporally (e.g., rainfall or temperature patterns). For example, some studies (
GIS models can be used not only to determine food safety risk factors and help identify possible interventions to reduce risks but also to understand trade-offs involved in such interventions. For example, Karp et al. (
Agent-based models
ABMs can be used to characterize the dynamics of pathogens in complex environments by considering events that can directly or indirectly influence pathogen introduction, persistence, die-off, or removal. While ABMs have been used to understand pathogen transmission in agricultural environments, for example, in grazing cattle (
ABMs can also support decision-making by estimating costs and different trade-offs. For instance, increasing wet cleaning frequency may enhance sanitation but also increase the risk of pathogen spread due to water dispersion (
AI-based models and predictive tools
AI tools, including machine learning models, are also increasingly being developed for food safety applications (
Neural networks have also been used to predict the growth/no-growth boundary of foodborne pathogens such as Staphylococcus aureus (
Emerging tools for precision food safety
Advances in technologies such as genomics offer opportunities to improve risk assessments and develop precision food safety approaches—methods that are more targeted and data-driven than current practices, akin to precision medicine (
Food safety regulations rarely incorporate strain-level virulence differences. A recent WHO/FAO report acknowledged the potential benefits of such precision but also highlighted challenges, including risk communication and the cost of subtype-specific management (
Trade-off risk assessments: current status and future developments
In the long term, a holistic approach to food safety (Figure 6) requires assessing both the benefits and costs of interventions—including the economic, environmental, societal, legal, and logistical considerations associated with different control strategies. Currently, most cost evaluations of food safety interventions occur after classical MC-QMRAs, which focus primarily on food safety outcomes. In some countries, regulatory impact assessments are required for high-cost regulations, but these are often qualitative and lack the methodological rigor (e.g., Monte Carlo simulations) of the initial MC-QMRA. Similarly, industry-led assessments typically consider costs only after the primary risk analysis, even though decisions on implementing food safety measures are often shaped as much by trade-offs as by the expected safety benefits.
Figure 6

A holistic approach to food safety decision-making. Key aspects for holistic decision-making are (i) modeling tools for microbial risk assessment, (ii) emerging precision food safety tools [e.g. genomic and other omics tools, model systems (e.g., SHIME—Simulator of Human Intestinal Microbial Ecosystem), and in vivo experiments], (iii) comprehensive trade-off assessments considering costs and benefits, and (iv) artificial intelligence-assisted risk negotiation.
Hence, there is a need for formal “trade-off risk assessments” that evaluate public health, environmental, social, and economic consequences of interventions within the risk assessment itself (see Appendix 1 for a list of terms that are relevant to trade-off risk assessments). Trade-off risk assessments represent one analytic approach that can be used to perform risk–benefit analyses (RBA), which can also be performed with more informal approaches. The term “multi-objective optimization” (a tool that can support “multiple-criteria decision-making”) represents another, related concept that has been mentioned in efforts to optimize food systems while considering multiple factors and trade-offs (
In food safety, trade-off risk assessments have been used for chemical hazards. For example, the FDA’s 2014 Quantitative assessment of the net effects on fetal neurodevelopment from eating commercial fish calculated the “net effects” of fish consumption by weighing the risks of methylmercury exposure against the benefits of nutrient intake during pregnancy using dual dose–response models (
Innovative approaches to socially acceptable food safety
As discussed, conventional risk assessment frameworks often fall short in addressing intersectoral trade-offs and the inherent complexity of achieving and defining appropriate levels of food safety in multi-sectoral food systems. A central challenge is the difficulty of comparing benefits and costs that are measured in different units, such as “illness cases avoided” versus “greenhouse gas emissions generated” or “implementation costs incurred”. Classical approaches attempt to harmonize these using common metrics, such as financial costs or DALYs. For example, one study assessed trade-offs between foodborne illness and the climate change impacts of two municipal water management plans, using DALYs as a shared metric (
However, using a single, shared metric for costs and benefits is often impractical and insufficient. In addition, risk perception by the general population also needs to be considered when trying to define acceptable food safety risks. To address this, Ehling-Schulz et al. (
By incorporating AI-assisted risk negotiation, food safety governance can become more adaptive, participatory, and transparent. This has the potential to improve risk communication and stakeholder trust as well as to enhance global food system resilience by fostering equitable and sustainable food safety solutions that accommodate societal needs. It is, however, important to consider that generative AI can be susceptible to fallacies including fabrication, and reasoning and mathematical errors (
Future directions
While risk assessments have a long history of supporting food safety decision-making, most have focused on quantifying risks and evaluating risk reduction strategies, often without formally accounting for the associated costs or trade-offs or addressing factors considered more subjective, such as consumer risk perception (which may often reflect social and cultural factors, such as the importance of specific foods and food preparation practices for a given society). In contrast, fields such as emergency preparedness are moving toward impact forecasting (
While there are advantages to globally consistent food safety standards (e.g., for trade), trade-off decisions will likely have to consider whether a single food safety standard is socially acceptable in different regions with distinct societal expectations and needs. What is considered an acceptable risk or sustainable outcome in one context may not be in another. Tools such as multicriteria decision analysis can integrate diverse data and preferences, including health impacts, costs, and societal acceptability (
Statements
Data availability statement
The original contributions presented in the study are included in the article. Further inquiries can be directed to the corresponding author.
Author contributions
MW: Conceptualization, Funding acquisition, Project administration, Supervision, Visualization, Writing – original draft, Writing – review & editing.
SS: Project administration, Visualization, Writing – original draft, Writing – review & editing.
AIM-S: Writing – original draft, Writing – review & editing.
KV: Writing – original draft, Writing – review & editing.
SJ: Funding acquisition, Writing – original draft, Writing – review & editing.
Funding
The authors declared that financial support was received for this work and/or its publication. This work was partially supported by the United States Department of Agriculture, National Institute of Food and Agriculture, Specialty Crop Research Initiative (project award no. 2019-03139), the Artificial Intelligence Institute for Next Generation Food Systems (AIFS) (USDA-NIFA no. 2020-67021-32855), Cornell Institute for Digital Agriculture (CIDA; no. NYC-143301). SJ acknowledges funding by the Swiss National Science Foundation (SNSF) as part of the MicRISK2030 project (Sinergia grant no. CVRSII5_209253). The funders were not involved in the study design, collection, analysis, interpretation of data, the writing of this article or the decision to submit it for publication.
Conflict of interest
MW serves as principal of Cayuga Food Safety Consulting, which includes, but is not limited to, serving on a food safety advisory council for Mars, Conagra, and Boarshead, and as a consultant for Neogen, BioMerieux, and Taylor Farms. KV is a principal of UniFAHS. The companies were not involved in the study design, collection, analysis, interpretation of data, the writing of this article, or the decision to submit it for publication.
The remaining authors declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The handling editor CE declared that he serves on the same advisory board for Mars Corporation as author MW and also on the advisory board of Neogen Corporation.
The Frontiers in Science Editorial Office assisted in the conceptualization of Figures 5, 6 in this article.
Generative AI statement
The authors declared that generative AI was not used in the creation of this manuscript.
Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.
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All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Author disclaimer
Any opinions, findings, conclusions, or recommendations expressed in this publication are those of the author(s) and should not be construed to represent any official United States or Swiss governments’ determination or policy.
References
1
World Health Organization. WHO Global Strategy for Food Safety 2022–2030: towards stronger food safety systems and global cooperation. Geneva: WHO (2022). Available at: https://www.who.int/publications/i/item/9789240057685
2
World Health Organization. WHO estimates of the global burden of foodborne diseases: foodborne disease burden epidemiology reference group 2007–2015. Geneva: WHO (2015). Available at: https://iris.who.int/bitstream/handle/10665/199350/9789241565165_eng.pdf
3
World Health Organization. WHO’s first ever global estimates of foodborne diseases find children under 5 account for almost one third of deaths [online]. (2015). Available at: https://www.who.int/news/item/03-12-2015-who-s-first-ever-global-estimates-of-foodborne-diseases-find-children-under-5-account-for-almost-one-third-of-deaths
4
JaffeeSHensonSUnnevehrLGraceDCassouE. The Safe Food Imperative: accelerating progress in low- and middle-income countries. Washington, DC: World Bank (2019). doi: 10.1596/978-1-4648-1345-0
5
World Food Programme. WFP and the sustainable development goals [online]. Available at: https://www.wfp.org/sdgs
6
ZwieteringMHGarreAWiedmannMBuchananRL. All food processes have a residual risk, some are small, some very small and some are extremely small: zero risk does not exist. Curr Opin Food Sci (2021) 39:83–92. doi: 10.1016/j.cofs.2020.12.017
7
Organisation for Economic Co-operation and Development. Safety evaluation of foods derived by modern biotechnology: concepts and principles. OECD (1993). Available at: https://www.iatp.org/sites/default/files/Safety_Evaluation_of_Foods_Derived_by_Modern_B.htm
8
GorrisL. Performance objectives and performance criteria – Two sides of the food chain. Mitt Lebensm Hyg (2004) 95:21–7. Available at: https://www.icmsf.org/wp-content/uploads/2018/02/021-027_Gorris.pdf
9
de SwarteCDonkerRA. Towards an FSO/ALOP based food safety policy. Food Control (2005) 16:825–30. doi: 10.1016/j.foodcont.2004.10.023
10
PetersonM. What is a de minimis risk? Risk Manag (2002) 4:47–55. doi: 10.1057/palgrave.rm.8240118
11
FarberJMZwieteringMWiedmannMSchaffnerDHedbergCWHarrisonMAet al. Alternative approaches to the risk management of Listeria monocytogenes in low risk foods. Food Control (2021) 123:107601. doi: 10.1016/j.foodcont.2020.107601
12
BuchananRL. Principles of risk analysis as applied to microbial food safety concerns. Mitt Lebensm Hyg (2004) 95:6–12. Available at: https://www.icmsf.org/wp-content/uploads/2018/02/006-012_Buchanan.pdf
13
Codex Alimentarius Commission. Principles and guidelines for the establishment and application of microbiological criteria related to foods (2013 edition). United Nations Food and Agriculture Organization (1993). Available at: https://www.fao.org/fao-who-codexalimentarius/sh-proxy/en/?lnk=1&url=https%253A%252F%252Fworkspace.fao.org%252Fsites%252Fcodex%252FStandards%252FCXG%2B21-1997%252FCXG_021e.pdf
14
DoménechEMartorellS. Definition and usage of food safety margins for verifying compliance of Food Safety Objectives. Food Control (2016) 59:669–74. doi: 10.1016/j.foodcont.2015.05.042
15
United States Food and Drug Administration. A quantitative assessment of the net effects on fetal neurodevelopment from eating commercial fish (as measured by IQ and also by early age verbal development in children). US FDA (2014). Available at: https://www.fda.gov/media/88491/download
16
ScallanEHoekstraRMAnguloFJTauxeRVWiddowsonMARoySLet al. Foodborne illness acquired in the United States-Major pathogens. Emerg Infect Dis (2011) 17:7–15. doi: 10.3201/eid1701.P11101
17
KoopmansMDuizerE. Foodborne viruses: an emerging problem. Int J Food Microbiol (2004) 90:23–41. doi: 10.1016/S0168-1605(03)00169-7
18
KaperJBNataroJPMobleyHLT. Pathogenic Escherichia coli. Nat Rev Microbiol (2004) 2:123–40. doi: 10.1038/nrmicro818
19
LeimbachAHackerJDobrindtU. E. coli as an all-rounder: the thin line between commensalism and pathogenicity. In: DobrindtUHackerJHSvanborgC, editors. Between pathogenicity and commensalism (1st edition). Berlin: Springer (2013). 3–32. doi: 10.1007/82_2012_303
20
McCarthyNGieseckeJ. Incidence of Guillain-Barré syndrome following infection with Campylobacter jejuni. Am J Epidemiol (2001) 153:610–4. doi: 10.1093/aje/153.6.610
21
Scallan WalterEJCrimSMBruceBBGriffinPM. Incidence of Campylobacter-associated Guillain-Barré syndrome estimated from health insurance data. Foodborne Pathog Dis (2020) 17:23–8. doi: 10.1089/fpd.2019.2652
22
American College of Rheumatology. Reactive arthritis [online]. Available at: https://rheumatology.org/patients/reactive-arthritis
23
TownesJM. Reactive arthritis after enteric infections in the United States: the problem of definition. Clin Infect Dis (2010) 50:247–54. doi: 10.1086/649540
24
Pogreba-BrownKAusthofETangXTrejoMJOwusu-DommeyABoydKet al. Enteric pathogens and reactive arthritis: systematic review and meta-analyses of pathogen-associated reactive arthritis. Foodborne Pathog Dis (2021) 18:627–39. doi: 10.1089/fpd.2020.2910
25
CheckleyWBuckleyGGilmanRHAssisAMGuerrantRLMorrisSSet al. Multi-country analysis of the effects of diarrhoea on childhood stunting. Int J Epidemiol (2008) 37:816–30. doi: 10.1093/ije/dyn099
26
KnielKEKumarDThakurS. Understanding the complexities of food safety using a “One Health” approach. Microbiol Spectr (2018) 6:401–11. doi: 10.1128/microbiolspec.pfs-0021-2017
27
ShaQForstnerMRJHahnD. Diversity of Salmonella in biofilms and water in a headwater ecosystem. FEMS Microbiol Ecol (2013) 83:642–9. doi: 10.1111/1574-6941.12021
28
YanamalaSMillerMFLoneraganGHGraggSEBrashearsMM. Potential for microbial contamination of spinach through feedyard air/dust growing in close proximity to cattle feedyard operationS. J Food Saf (2011) 31:525–9. doi: 10.1111/j.1745-4565.2011.00330.x
29
KumarGDWilliamsRCAl QublanHMSriranganathanNBoyerRREifertJD. Airborne soil particulates as vehicles for Salmonella contamination of tomatoes. Int J Food Microbiol (2017) 243:90–5. doi: 10.1016/j.ijfoodmicro.2016.12.006
30
LangholzJAJay-RussellMT. Potential role of wildlife in pathogenic contamination of fresh produce. Hum Wildl Interac (2013) 7:140–57. doi: 10.26077/e5gg-r037
31
ParkSNavratilSGregoryABauerASrinathISzonyiBet al. Multifactorial effects of ambient temperature, precipitation, farm management, and environmental factors determine the level of generic Escherichia coli contamination on preharvested spinach. Appl Environ Microbiol (2015) 81:2635–50. doi: 10.1128/AEM.03793-14
32
EvenBThaiHTMPhamHTMBénéC. Defining barriers to food systems sustainability: a novel conceptual framework. Front Sustain Food Syst (2024) 8:1453999. doi: 10.3389/fsufs.2024.1453999
33
RittelHWJWebberMM. Dilemmas in a general theory of planning. Policy Sci (1973) 4:155–69. doi: 10.1007/BF01405730
34
LönngrenJvan PoeckK. Wicked problems: a mapping review of the literature. Int J Sust Dev World Ecol (2021) 28:481–502. doi: 10.1080/13504509.2020.1859415
35
Statista. Number of chickens worldwide from 1990 to 2023 (in million animals)* [online] (2025). Available at: https://www.statista.com/statistics/263962/number-of-chickens-worldwide-since-1990/
36
Statista. Per capita consumption of fresh vegetables in the United States in 2023, by vegetable type (in pounds)* [online] (2024). Available at: https://www.statista.com/statistics/257345/per-capita-consumption-of-fresh-vegetables-in-the-us-by-type/
37
Food and Agriculture Organization of the United Nations. Feeding the world in 2050. Rome: FAO (2009). Available at: https://www.fao.org/4/k6021e/k6021e.pdf
38
Van DijkMMorleyTRauMLSaghaiY. A meta-analysis of projected global food demand and population at risk of hunger for the period 2010–2050. Nat Food (2021) 2:494–501. doi: 10.1038/s43016-021-00322-9
39
PetruzziLCampanielloDSperanzaBCorboMRSinigagliaMBevilacquaA. Thermal treatments for fruit and vegetable juices and beverages: a literature overview. Compr Rev Food Sci Food Saf (2017) 16:668–91. doi: 10.1111/1541-4337.12270
40
PiersonMDSmootLA. Nitrite, nitrite alternatives, and the control of Clostridium botulinum in cured meats. Crit Rev Food Sci Nutr (1983) 17:141–87. doi: 10.1080/10408398209527346
41
SongPWuLGuanW. Dietary nitrates, nitrites, and nitrosamines intake and the risk of gastric cancer: a meta-analysis. Nutrients (2015) 7:9872–95. doi: 10.3390/nu7125505
42
De MeyEDe MaereHPaelinckHFraeyeI. Volatile N-nitrosamines in meat products: potential precursors, influence of processing, and mitigation strategies. Crit Rev Food Sci Nutr (2017) 57:2909–23. doi: 10.1080/10408398.2015.1078769
43
BondonnoCPZhongLBondonnoNPSimMBlekkenhorstLCLiuAet al. Nitrate: the Dr. Jekyll and Mr. Hyde of human health? Trends Food Sci Technol (2023) 135:57–73. doi: 10.1016/j.tifs.2023.03.014
44
BurtonNCGibbinsJ. Assessment of peracetic acid exposure among federal poultry inspectors. United States Department of Health and Human Services (2016). Available at: https://www.cdc.gov/niosh/hhe/reports/pdfs/2014-0196-3254.pdf
45
KarpDSBaurPAtwillERDe MasterKGennetSIlesAet al. The unintended ecological and social impacts of food safety regulations in California’s central coast region. Bioscience (2015) 65:1173–83. doi: 10.1093/biosci/biv152
46
MartinNHTrmčićAHsiehTHBoorKJWiedmannM. The evolving role of coliforms as indicators of unhygienic processing conditions in dairy foods. Front Microbiol (2016) 7:1549. doi: 10.3389/fmicb.2016.01549
47
AnelichLECMLuesRFarberJMParreiraVR. SARS-CoV-2 and risk to food safety. Front Nutr (2020) 7:580551. doi: 10.3389/fnut.2020.580551
48
KitzRWalkerTCharleboisSMusicJ. Food packaging during the COVID-19 pandemic: consumer perceptions. Int J Consum Stud (2022) 46:434–48. doi: 10.1111/ijcs.12691
49
KrugMDChapmanBDanylukMD. Establishing a lot through sanitation clean breaks in produce packing facilities (2020 edition). University of Florida Institute of Food and Agricultural Sciences (2013). Available at: https://www.citrusindustry.net/wp-content/uploads/2024/02/FS234.pdf
50
ZaragozaA. As Big Beer moves in, activists in Mexicali fight to keep their water. National Public Radio (2018). Available at: https://www.npr.org/sections/thesalt/2018/03/26/596448290/as-big-beer-moves-in-activists-in-mexicali-fight-to-keep-their-water
51
HouserMDorfmanJHRejesusRM. The long-term effects of meat recalls on futures markets. Appl Econ Perspect Policy (2019) 41:235–48. doi: 10.1093/aepp/ppy010
52
BarlowSMBoobisARBridgesJCockburnADekantWHepburnPet al. The role of hazard- and risk-based approaches in ensuring food safety. Trends Food Sci Technol (2015) 46:176–88. doi: 10.1016/j.tifs.2015.10.007
53
SsemandaJNden BestenHMWvan WagenbergCPAZwieteringMH. Quantitative assessment of food safety interventions for Campylobacter spp. and Salmonella spp. along the chicken meat supply chain in Burkina Faso and Ethiopia. Int J Food Microbiol (2024) 415:110637. doi: 10.1016/j.ijfoodmicro.2024.110637
54
American Academy of Microbiology. Clean Water: what is acceptable microbial risk? Washington, DC: American Society for Microbiology (2007). Available at: https://www.ncbi.nlm.nih.gov/books/NBK560444/
55
World Trade Organization. The WTO Agreement on the application of sanitary and phytosanitary measures (SPS Agreement). WTO (1995). Available at: https://www.wto.org/english/tratop_e/sps_e/spsagr_e.htm
56
ZwieteringMHJacxsensLMembréJMNautaMPeterzM. Relevance of microbial finished product testing in food safety management. Food Control (2016) 60:31–43. doi: 10.1016/j.foodcont.2015.07.002
57
Unites States National Archives and Records Administration’s Office of the Federal Register, United States Government Publishing Office. Current good manufacturing practice, hazard analysis, and risk-based preventive controls for human food [part 117]. In: Code of Federal Regulations. OFR (2015). Available at: https://www.ecfr.gov/current/title-21/chapter-I/subchapter-B/part-117
58
LepperJAhnSSchneiderKRDanylukMDGoodrich-SchneiderR. The Food Safety Modernization Act of 2011: final rule for preventive controls for human food: FSHN17-6/FS301, 1/2018. EDIS (2018) 2018(1). doi: 10.32473/edis-fs301-2018
59
FarakosSMSPouillotRJohnsonRSpungenJSonIAndersonNet al. A quantitative assessment of the risk of human salmonellosis arising from the consumption of almonds in the United States: the impact of preventive treatment levels. J Food Prot (2017) 80:863–78. doi: 10.4315/0362-028X.JFP-16-403
60
United States Food and Drug Administration. Risk assessments: Salmonella on tree nuts [online] (2017). Available at: https://www.fda.gov/food/risk-and-safety-assessments-food/risk-assessments-salmonella-tree-nuts
61
United Fresh Food Safety & Technology Council. Guidance on environmental monitoring and control of Listeria for the fresh produce industry. Second edition. Washington, DC: United Fresh Produce Association (2018). Available at: https://www.freshproduce.com/siteassets/files/reports/food-safety/guidance-on-environmental-monitoring-and-control-of-listeria.pdf
62
FrankRHBernankeBS. Principles of macroeconomics (4th edition). New York, NY: McGraw-Hill Irwin (2009).
63
XueYGengXKipropEHongM. How do spillover effects influence the food safety strategies of companies? New orientation of regulations for food safety. Foods (2021) 10:1–17. doi: 10.3390/foods10020451
64
SolbergCTSørheimPMüllerKEGamlundENorheimOFBarraM. The devils in the DALY: prevailing evaluative assumptions. Public Health Ethics (2020) 13:259–74. doi: 10.1093/phe/phaa030
65
NakaoYKawakamiHMiyazakiSSaitoMLuoYYamamotoKet al. Evaluation of health utility in trial-based cost-utility analyses for major cardiovascular disease: protocol for a systematic review. BMJ Open (2023) 13:e067045. doi: 10.1136/bmjopen-2022-067045
66
DevleesschauwerBScharffRLKowalcykBBHavelaarAH. Burden and risk assessment of foodborne disease. In: RobertsT, editor. Food safety economics: incentives for a safer food supply (1st edition). Cham: Springer International Publishing (2018). 83–106. doi: 10.1007/978-3-319-92138-9_6
67
FengXKimDDCohenJTNeumannPJOllendorfDA. Using QALYs versus DALYs to measure cost-effectiveness: how much does it matter? Int J Technol Assess Health Care (2020) 36:96–103. doi: 10.1017/S0266462320000124
68
GoldMRStevensonDFrybackDG. HALYs and QALYs and DALYs, oh my: similarities and differences in summary measures of population health. Annu Rev Public Health (2002) 23:115–34. doi: 10.1146/annurev.publhealth.23.100901.140513
69
PozoVFSchroederTC. Evaluating the costs of meat and poultry recalls to food firms using stock returns. Food Policy (2016) 59:66–77. doi: 10.1016/j.foodpol.2015.12.007
70
GomezCBMarksBP. Monetizing the impact of food safety recalls on the low-moisture food industry. J Food Prot (2020) 83:829–35. doi: 10.4315/JFP-19-553
71
RiberaLAPalmaMAPaggiMKnutsonRMasabniJGAncisoJ. Economic analysis of food safety compliance costs and foodborne illness outbreaks in the United States. HortTechnology (2012) 22:150–6. doi: 10.21273/HORTTECH.22.2.150
72
BartschSMAstiLNyathiSSpikerMLLeeBY. Estimated cost to a restaurant of a foodborne illness outbreak. Public Health Rep (2018) 133:274–86. doi: 10.1177/0033354917751129
73
ThomasMKVriezenRFarberJMCurrieASchlechWFazilA. Economic cost of a Listeria monocytogenes outbreak in Canada 2008. Foodborne Pathog Dis (2015) 12:966–71. doi: 10.1089/fpd.2015.1965
74
PangHLambertiniEBuchananRLSchaffnerDWPradhanAK. Quantitative microbial risk assessment for Escherichia coli O157:H7 in fresh-cut lettuce. J Food Prot (2017) 80:302–11. doi: 10.4315/0362-028X.JFP-16-246
75
LambertiniEBaroueiJSchaffnerDWDanylukMDHarrisLJ. Modeling the risk of salmonellosis from consumption of pistachios produced and consumed in the United States. Food Microbiol (2017) 67:85–96. doi: 10.1016/j.fm.2017.06.003
76
SsemandaJNden BestenHMWDioneMMAmenuKKnight-JonesTJDZwieteringMHet al. Cost-effectiveness of interventions toward improving microbial food safety of chicken meat along supply chains in Burkina Faso and Ethiopia. Int J Food Microbiol (2025) 431:111086. doi: 10.1016/j.ijfoodmicro.2025.111086
77
GellynckXMessensWHaletDGrijspeerdtKHartnettEViaeneJ. Economics of reducing Campylobacter at different levels within the Belgian poultry meat chain. J Food Prot (2008) 71:479–85. doi: 10.4315/0362-028X-71.3.479
78
Codex Alimentarius Committee. Guidelines on the application of general principles of food hygiene to the control of Listeria monocytogenes in foods. Rome: United Nations Food and Agriculture Organization (2007). Available at: https://www.fao.org/fao-who-codexalimentarius/sh-proxy/en/?lnk=1&url=https%253A%252F%252Fworkspace.fao.org%252Fsites%252Fcodex%252FStandards%252FCXG%2B61-2007%252FCXG_061e.pdf
79
GlassKBedaleWUnruhD. It’s time to reformulate deli meats to reduce the risk of Listeria monocytogenes. Food Safety Magazine. (2024). Available at: https://www.food-safety.com/articles/9992-its-time-to-reformulate-deli-meats-to-reduce-the-risk-of-listeria-monocytogenes
80
United States Department of AgricultureFood Safety and Inspection Service. Controlling Listeria monocytogenes in post-lethality exposed ready-to-eat meat and poultry products. USDA FSIS (2014). Available at: https://www.fsis.usda.gov/guidelines/2014-0001
81
GottliebSLNewbernECGriffinPMGravesLMHoekstraRMBakerNLet al. Multistate outbreak of listeriosis linked to Turkey deli meat and subsequent changes in US regulatory policy. Clin Infect Dis (2006) 42:29–36. doi: 10.1086/498113
82
CartwrightEJJacksonKAJohnsonSDGravesLMSilkBJMahonBE. Listeriosis outbreaks and associated food vehicles, United States 1998–2008. Emerg Infect Dis (2013) 19:1–9. doi: 10.3201/eid1901.120393
83
United States Department of Agriculture Food Safety and Inspection Service. FSIS Directive 10,240.4, revision 4: Listeria rule verification activities. USDA FSIS (2022). Available at: https://www.fsis.usda.gov/sites/default/files/media_file/2020-08/10240.4.pdf
84
PradhanAKIvanekRGröhnYGeornarasISofosJNWiedmannM.Quantitative risk assessment for Listeria monocytogenes in selected categories of deli meats: impact of lactate and diacetate on listeriosis cases and deaths. J Food Prot (2009) 72:978–89. doi: 10.4315/0362-028X-72.5.978
85
United States Department of AgricultureFood Safety and Inspection Service. Comparative risk assessment for Listeria monocytogenes in ready-to-eat meat and poultry deli meats report. USDA FSIS (2010). Available at: https://www.fsis.usda.gov/sites/default/files/media_file/2020-07/Comparative_RA_Lm_Report_May2010.pdf
86
EFSA Panel on Biological Hazards (BIOHAZ)RicciAChemalyMDaviesRFernández EscámezPSGironesRet al. Hazard analysis approaches for certain small retail establishments in view of the application of their food safety management systems. EFSA J (2017) 15:e04697. doi: 10.2903/j.efsa.2017.4697
87
United States Food and Drug Administration. Control of Listeria monocytogenes in ready-to-eat foods: guidance for industry. Draft guidance. US FDA (2017). Available at: https://www.fda.gov/media/102633/download
88
European Association of Fruit and Vegetable Processors. Hygiene guidelines for the control of Listeria monocytogenes in the production of quick-frozen vegetables. Brussels: PROFEL (2020). Available at: https://profel-europe.eu/_library/_files/PROFEL_Listeria_mono_guidelines_November2020.pdf
89
United States Food and Drug Administration, United States Department of Agriculture. Quantitative assessment of relative risk to public health from foodborne Listeria monocytogenes among selected categories of ready-to-eat foods. US FDA (2003). Available at: https://www.fda.gov/media/124721/download?attachment
90
ZoellnerCWiedmannMIvanekR. An assessment of listeriosis risk associated with a contaminated production lot of frozen vegetables consumed under alternative consumer handling scenarios. J Food Prot (2019) 82:2174–93. doi: 10.4315/0362-028X.JFP-19-092
91
BuchananRL. Microbiological risk assessment: origins, current status, and future challenges. Food Safety Magazine (2021). Available at: https://www.food-safety.com/articles/1754-cover-story-microbiological-risk-assessment-origins-current-status-and-future-challenges
92
HaasCN. Microbial dose response modeling: past, present, and future. Environ Sci Technol (2015) 49:1245–59. doi: 10.1021/es504422q
93
United States Department of Agriculture Food Safety and Inspection Service, United States Environmental Protection Agency. Microbial risk assessment guideline: pathogenic organisms with focus on food and water. USDA FSIS (2012). Available at: https://www.fsis.usda.gov/sites/default/files/media_file/2020-07/Microbial_Risk_Assessment_Guideline_2012-001.pdf
94
PouillotRDelignette-MullerML. Evaluating variability and uncertainty separately in microbial quantitative risk assessment using two R packages. Int J Food Microbiol (2010) 142:330–40. doi: 10.1016/j.ijfoodmicro.2010.07.011
95
FarakosSMSPouillotRDavidsonGRJohnsonRSpungenJSonIet al. A quantitative risk assessment of human salmonellosis from consumption of pistachios in the United States. J Food Prot (2018) 81:1001–14. doi: 10.4315/0362-028X.JFP-17-379
96
HopeBKBakerAREdelEDHogueATSchlosserWDWhitingRet al. An overview of the Salmonella enteritidis risk assessment for shell eggs and egg products. Risk Anal (2002) 22:203–18. doi: 10.1111/0272-4332.00023
97
United States Department of Agriculture Food Safety and Inspection Service. Salmonella Enteritidis risk assessment: shell eggs and egg products. USDA FSIS (1998). Available at: https://www.fsis.usda.gov/sites/default/files/media_file/2020-07/pdfrisk1.pdf
98
Food and Agriculture Organization of the United Nations, World Health Organization. Risk assessment of Listeria monocytogenes in ready to eat foods. Rome: FAO (2004). Available at: https://www.fao.org/fileadmin/templates/agns/pdf/jemra/mra4_en.pdf
99
United States Department of Agriculture Food Safety and Inspection Service. Quantitative risk assessment for Salmonella in raw chicken and raw chicken products. USDA FSIS (2024). Available at: https://www.fsis.usda.gov/sites/default/files/media_file/documents/Chicken_SRA_July2024.pdf
100
ChenROrsiRHGuariglia-OropezaVWiedmannM. Development of a modeling tool to assess and reduce regulatory and recall risks for cold-smoked salmon due to Listeria monocytogenes contamination. J Food Prot (2022) 85:1335–54. doi: 10.4315/JFP-22-025
101
PintoGReyesGABarnett-NeefsCJungYJQianCWiedmannMet al. Development of a flexible produce supply chain food safety risk model: comparing tradeoffs between improved process controls and additional product testing for leafy greens as a test case. J Food Prot (2025) 88:100393. doi: 10.1016/j.jfp.2024.100393
102
GaoSLewisGDAshokkumarMHemarY. Inactivation of microorganisms by low-frequency high-power ultrasound: a simple model for the inactivation mechanism. Ultrason Sonochem (2014) 21:454–60. doi: 10.1016/j.ultsonch.2013.06.007
103
StrawnLKFortesEDBihnEANightingaleKKGröhnYTWoroboRWet al. Landscape and meteorological factors affecting prevalence of three food-borne pathogens in fruit and vegetable farms. Appl Environ Microbiol (2013) 79:588–600. doi: 10.1128/AEM.02491-12
104
ChapinTKNightingaleKKWoroboRWWiedmannMStrawnLK. Geographical and meteorological factors associated with isolation of Listeria species in New York state produce production and natural environments. J Food Prot (2014) 77:1919–28. doi: 10.4315/0362-028X.JFP-14-132
105
WellerDWiedmannMStrawnLK. Spatial and temporal factors associated with an increased prevalence of Listeria monocytogenes in spinach fields in New York state. Appl Environ Microbiol (2015) 81:6059–69. doi: 10.1128/AEM.01286-15
106
KarpDSGennetSKilonzoCPartykaMChaumontNAtwillERet al. Comanaging fresh produce for nature conservation and food safety. Proc Natl Acad Sci USA (2015) 112:11126–31. doi: 10.1073/pnas.1508435112
107
DawsonDEKeungJHNapolesMGVellaMRChenSSandersonMWet al. Investigating behavioral drivers of seasonal Shiga-Toxigenic Escherichia coli (STEC) patterns in grazing cattle using an agent-based model. PloS One (2018) 13:e0205418. doi: 10.1371/journal.pone.0205418
108
ZoellnerCJenningsRWiedmannMIvanekR. EnABLe: an agent-based model to understand Listeria dynamics in food processing facilities. Sci Rep (2019) 9:495. doi: 10.1038/s41598-018-36654-z
109
JungYJQianCBarnett-NeefsCIvanekRWiedmannM. Developing an agent-based model that predicts Listeria spp. transmission to assess Listeria control strategies in retail stores. J Food Prot (2024) 87:100337. doi: 10.1016/j.jfp.2024.100337
110
MokhtariAVan DorenJM. An agent-based model for pathogen persistence and cross-contamination dynamics in a food facility. Risk Anal (2019) 39:992–1021. doi: 10.1111/risa.13215
111
Barnett-NeefsCWiedmannMIvanekR. Examining patterns of persistent Listeria contamination in packinghouses using agent-based models. J Food Prot (2022) 85:1824–41. doi: 10.4315/JFP-22-119
112
KaruppuchamyVHeldmanDRSnyderAB. A review of food safety in low-moisture foods with current and potential dry-cleaning methods. J Food Sci (2024) 89:793–810. doi: 10.1111/1750-3841.16920
113
QianCMurphySIOrsiRHWiedmannM. How can AI help improve food safety? Annu Rev Food Sci Technol (2023) 14:517–38. doi: 10.1146/annurev-food-060721-013815
114
ChhetriKB. Applications of artificial intelligence and machine learning in food quality control and safety assessment. Food Eng Rev (2024) 16:1–21. doi: 10.1007/s12393-023-09363-1
115
WellerDLLoveTMTWiedmannM. Comparison of resampling algorithms to address class imbalance when developing machine learning models to predict foodborne pathogen presence in agricultural water. Front Environ Sci (2021) 9:701288. doi: 10.3389/fenvs.2021.701288
116
ChungTYanRWellerDLKovacJ. Conditional forest models built using metagenomic data accurately predicted Salmonella contamination in northeastern streams. Microbiol Spectr (2023) 11:e00381–23. doi: 10.1128/spectrum.00381-23
117
TonnerPDDarnellCLEngelhardtBESchmidAK. Detecting differential growth of microbial populations with Gaussian process regression. Genome Res (2017) 27:320–33. doi: 10.1101/gr.210286.116
118
NjagePMKLeekitcharoenphonPHaldT. Improving hazard characterization in microbial risk assessment using next generation sequencing data and machine learning: predicting clinical outcomes in shigatoxigenic Escherichia coli. Int J Food Microbiol (2019) 292:72–82. doi: 10.1016/j.ijfoodmicro.2018.11.016
119
KamilMZTaleb-BerrouaneMKhanFAmyottePAhmedS. Textual data transformations using natural language processing for risk assessment. Risk Anal (2023) 43:2033–52. doi: 10.1111/risa.14100
120
Fernández-NavarroFValeroAHervás-MartínezCGutiérrezPAGarcía-GimenoRMZurera-CosanoG. Development of a multi-classification neural network model to determine the microbial growth/no growth interface. Int J Food Microbiol (2010) 141:203–12. doi: 10.1016/j.ijfoodmicro.2010.05.013
121
KovacJBakkerHCarrollLMWiedmannM. Precision food safety: a systems approach to food safety facilitated by genomics tools. Trends Analyt Chem (2017) 96:52–61. doi: 10.1016/j.trac.2017.06.001
122
United States Department of Agriculture Food Safety and Inspection Service. Expansion of FSIS shiga toxin-producing Escherichia coli (STEC) testing to additional raw beef products. USDA FSIS (2022). Available at: https://www.federalregister.gov/d/2022-25140
123
NightingaleKKWindhamKMartinKEYeungMWiedmannM. Select Listeria monocytogenes subtypes commonly found in foods carry distinct nonsense mutations in inlA, leading to expression of truncated and secreted internalin A, and are associated with a reduced invasion phenotype for human intestinal epithelial cells. Appl Environ Microbiol (2005) 71:8764–72. doi: 10.1128/AEM.71.12.8764-8772.2005
124
NightingaleKKIvyRAHoAJFortesEDNjaaBLPetersRMet al. inlA premature stop codons are common among Listeria monocytogenes isolates from foods and yield virulence-attenuated strains that confer protection against fully virulent strains. Appl Environ Microbiol (2008) 74:6570–83. doi: 10.1128/AEM.00997-08
125
ManuelCSSteltenAVWiedmannMNightingaleKKOrsiRH. Prevalence and distribution of Listeria monocytogenes inlA alleles prone to phase variation and inlA alleles with premature stop codon mutations among human, food, animal, and environmental isolates. Appl Environ Microbiol (2015) 81:8339–45. doi: 10.1128/AEM.02752-15
126
OrsiRHBakkerHCWiedmannM. Listeria monocytogenes lineages: genomics, evolution, ecology, and phenotypic characteristics. Int J Med Microbiol (2011) 301:79–96. doi: 10.1016/j.ijmm.2010.05.002
127
MauryMMTsaiYHCharlierCTouchonMChenal-FrancisqueVLeclercqAet al. Uncovering Listeria monocytogenes hypervirulence by harnessing its biodiversity. Nat Genet (2016) 48:308–13. doi: 10.1038/ng.3501
128
MauryMMChenal-FrancisqueVBracq-DieyeHHanLLeclercqAValesGet al. Spontaneous loss of virulence in natural populations of Listeria monocytogenes. Infect Immun (2017) 85:10–1128. doi: 10.1128/IAI.00541-17
129
MauryMMBracq-DieyeHHuangLValesGLavinaMThouvenotPet al. Hypervirulent Listeria monocytogenes clones’ adaption to mammalian gut accounts for their association with dairy products. Nat Commun (2019) 10:2488. doi: 10.1038/s41467-019-10380-0
130
Food and Agriculture Organization of the United Nations, World Health Organization. Listeria monocytogenes in ready-to-eat (RTE) foods: attribution, characterization and monitoring. Rome: FAO (2022). doi: 10.4060/cc2400en
131
KimMBarnett-NeefsCChavezRAKealeyEWiedmannMStasiewiczMJ. Risk assessment predicts most of the salmonellosis risk in raw chicken parts is concentrated in those few products with high levels of high-virulence serotypes of Salmonella. J Food Prot (2024) 87:100304. doi: 10.1016/j.jfp.2024.100304
132
StruelensMJLuddenCWernerGSintchenkoVJokelainenPIpM. Real-time genomic surveillance for enhanced control of infectious diseases and antimicrobial resistance. Front Sci (2024) 2:1298248. doi: 10.3389/fsci.2024.1298248
133
BerdenJHanley-CookGTChimeraBCakmakEKNicolasGBaudryJet al. Synergies between food biodiversity, processing levels, and the eat-lancet diet for nutrient adequacy and environmental sustainability: a multi-objective optimization using the EPIC cohort. Am J Clin Nutr (2025) 123:101115. doi: 10.1016/j.ajcnut.2025.11.006
134
DyeKCEggersJPShapiraZ. Trade-offs in a tempest: stakeholder influence on hurricane evacuation decisions. Organ Sci (2014) 25:1009–25. doi: 10.1287/orsc.2013.0890
135
DomonoskeC. Why didn’t officials order the evacuation of Houston. National Public Radio (2017). Available at: https://www.npr.org/sections/thetwo-way/2017/08/28/546721363/why-didn-t-officials-order-the-evacuation-of-houston
136
De HaesHAUSleeswijkAWHeijungsR. Similarities, differences and synergisms between HERA and LCA - an analysis at three levels. Hum Ecol Risk Assess (2006) 12:431–59. doi: 10.1080/10807030600561659
137
KobayashiYPetersGMAshboltNJHeimerssonSSvanströmMKhanSJ. Global and local health burden trade-off through the hybridisation of quantitative microbial risk assessment and life cycle assessment to aid water management. Water Res (2015) 79:26–38. doi: 10.1016/j.watres.2015.03.015
138
OlsenSIChristensenFMHauschildMPedersenFLarsenHFTùrslùvJ. Life cycle impact assessment and risk assessment of chemicals - a methodological comparison. Environ Impact Assess Rev (2001) 21:385–402. doi: 10.1016/S0195-9255(01)00075-0
139
HarderRHolmquistHMolanderSSvanströmMPetersGM. Review of environmental assessment case studies blending elements of risk assessment and life cycle assessment. Environ Sci Technol (2015) 49:13083–93. doi: 10.1021/acs.est.5b03302
140
KobayashiYPetersGMKhanSJ. Towards more holistic environmental impact assessment: hybridisation of life cycle assessment and quantitative risk assessment. Proc CIRP (2015) 29:378–83. doi: 10.1016/j.procir.2015.01.064
141
MotaJDOGuillouSPierreFMembréJM. Public health risk-benefit assessment of red meat in France: current consumption and alternative scenarios. Food Chem Toxicol (2021) 149:111994. doi: 10.1016/j.fct.2021.111994
142
TondoECGonçalvesCTH. Using risk-benefit analysis to control Salmonella in chicken meat. Food Qual Saf (2021) 5:970–1298. doi: 10.1093/fqsafe/fyab027
143
MembréJMSantillana FarakosSNautaM. Risk-benefit analysis in food safety and nutrition. Curr Opin Food Sci (2021) 39:76–82. doi: 10.1016/j.cofs.2020.12.009
144
RuzanteJMGriegerKWoodwardKLambertiniEKowalcykB. The use of multi-criteria decision analysis in food safety risk-benefit assessment. Food Prot Trends (2017) 37:132–9.
145
FarakosSMSPouillotRSpungenJFlanneryBVan DorenJMDennisS. Implementing a risk-risk analysis framework to evaluate the impact of food intake shifts on risk of illness: a case study with infant cereal. Food Addit Contam Part A (2021) 38:718–30. doi: 10.1080/19440049.2021.1885752
146
TchonkouangRDOnyeakaHNkoutchouH. Assessing the vulnerability of food supply chains to climate change-induced disruptions. Sci Total Environ (2024) 920:171047. doi: 10.1016/j.scitotenv.2024.171047
147
MirónIJLinaresCDíazJ. The influence of climate change on food production and food safety. Environ Res (2023). 216:114674. doi: 10.1016/j.envres.2022.114674
148
Ehling-SchulzMFilterMZinsstagJKoutsoumanisKEllouzeMTeichmannJet al. Risk negotiation: a framework for One Health risk analysis. Bull World Health Organ (2024) 102:453–6. doi: 10.2471/BLT.23.290672
149
SunYShengDZhouZWuY. AI hallucination: towards a comprehensive classification of distorted information in artificial intelligence-generated content. Humanit Soc Sci Commun (2024) 11:1–14. doi: 10.1057/s41599-024-03811-x
150
BickABlandinADemingDJLouisS. The rapid adoption of generative AI. Cambridge, MA: United States National Bureau of Economic Research. (2024) Available at: https://www.nber.org/system/files/working_papers/w32966/w32966.pdf
151
MerzBKuhlickeCKunzMPittoreMBabeykoABreschDNet al. Impact forecasting to support emergency management of natural hazards. Rev Geophys (2020) 58:e2020RG000704. doi: 10.1029/2020RG000704
152
DaleMWicksJMylneKPappenbergerFLaegerSTaylorS. Probabilistic flood forecasting and decision-making: an innovative risk-based approach. Nat Hazards (2014) 70:159–72. doi: 10.1007/s11069-012-0483-z
153
WildAJWilsonTMBebbingtonMSColeJWCraigHM. Probabilistic volcanic impact assessment and cost-benefit analysis on network infrastructure for secondary evacuation of farm livestock: a case study from the dairy industry, Taranaki, New Zealand. J Volcanol Geotherm Res (2019) 387:106670. doi: 10.1016/j.jvolgeores.2019.106670
154
DavidsonRANozickLKWachtendorfTBlantonBColleBKolarRLet al. An integrated scenario ensemble-based framework for hurricane evacuation modeling: part 1—decision support system. Risk Anal (2020) 40:97–116. doi: 10.1111/risa.12990
155
RichardsonJSchlanderM. Health technology assessment (HTA) and economic evaluation: efficiency or fairness first. J Mark Access Health Policy (2019) 7(1):1557981. doi: 10.1080/20016689.2018.1557981
156
CaroJJBrazierJEKarnonJKolominsky-RabasPMcGuireAJNordEet al. Determining value in health technology assessment: stay the course or tack away?Pharmacoeconomics (2019) 37:293–9. doi: 10.1007/s40273-018-0742-2
157
MccaugheyDBruningNS. Rationality versus reality: the challenges of evidence-based decision making for health policy makers. Implement Sci (2010) 5:1–13. doi: 10.1186/1748-5908-5-39
158
Food and Agriculture Organization of the United Nations, World Health Organization. Principles and guidelines for incorporating microbiological risk assessment in the development of food safety standard, guidelines and related texts. Rome: FAO (2002). Available at: https://www.who.int/publications/m/item/guidelines-for-incorporating-microbiological-risk-assessment-food-safety-standards
159
FerdousJBensebaaFMilaniASHewageKBhowmikPPelletierN. Development of a generic decision tree for the integration of Multi-Criteria Decision-Making (MCDM) and Multi-Objective Optimization (MOO) methods under uncertainty to facilitate sustainability assessment: a methodical review. Sustainability (2024) 16:2684. doi: 10.3390/su16072684
160
SendínJOHAlonsoAABangaJR. Efficient and robust multi-objective optimization of food processing: a novel approach with application to thermal sterilization. J Food Eng (2010) 98:317–24. doi: 10.1016/j.jfoodeng.2010.01.007
161
BanachJLZwieteringMHvan der Fels-KlerxHJ. Multi-criteria decision analysis to evaluate control strategies for preventing cross-contamination during fresh-cut lettuce washing. Food Control (2021) 128:108136. doi: 10.1016/j.foodcont.2021.108136
162
RuzanteJMWhitingRCDennisSBBuchananRL. Microbial risk assessment. In: DoyleMPBuchananRL, editors. Food microbiology: fundamentals and frontiers (4th edition). Washington, DC: ASM Press (2012). 225–6. doi: 10.1128/9781555818463.ch41
163
CelliniSRKeeJE. Cost-effectiveness and cost-benefit analysis. In: NewcomerKEHatryHPWholeyJS, editors. Handbook of practical program evaluation (4th edition). Hoboken, NJ: John Wiley & Sons (2015). 636–72. doi: 10.1002/9781119171386.ch24
Appendix
Appendix 1
| Concept | Abbreviation | Description |
|---|---|---|
| Agent-based model | ABM | Simulation models that represent the components of a system, such as a processing facility, as “agents” that can interact with one another based on rules or frameworks. ABMs have been used to understand factors that are involved in the transmission and control of pathogens in food processing or retail environments ( |
| As low as reasonably achievable | ALARA | A principle for setting food safety goals by (i) identifying what can be achieved with current risk management options and (ii) setting a goal that can thus be realistically achieved by a given risk management strategy ( |
| Appropriate level of protection | ALOP | The “level of protection” considered appropriate or the level of risk that is considered acceptable or tolerable for a given food-hazard pair ( |
| Food safety objective | FSO | “The maximum frequency and/or concentration of a (microbial) hazard in a food at the time of consumption that still provides the appropriate level of protection” ( |
| Multi-objective optimization | MOO | An optimization approach that is used to find the best solution to a problem while considering more than one objective function (i.e., factor) with conflicting goals ( |
| Multi-criteria decision analysis | MCDA | An approach that uses a decision matrix to characterize potential solutions to a problem across a set of standards (i.e., criteria) ( |
| Performance criteria | PC | “The effect of one or more control measure(s) needed to meet or contribute to meeting a PO [performance objective]” ( |
| Performance objectives | POs | “The maximum frequency and/or concentration of a (microbial) hazard in a food at a specified step in the food chain before time of consumption that still provides or contributes to the achievement of an FSO or ALOP, as applicable” ( |
| Quantitative microbial risk assessment | QMRA | A probabilistic framework that is typically used to estimate the population-level risk of foodborne microbial illness, considering various factors including consumption of a certain food, food processing and handling practices, or policy changes. This framework involves four steps: hazard identification, exposure assessment, dose-response characterization, and risk-characterization ( |
| Qualitative microbial risk assessment | NA1 | A framework that estimates population-level risk of microbial illness; the outcome is a risk score or category, which can be used to compare and rank practices. This approach is used either (i) as a first step during risk analysis (including to evaluate the need for a quantitative risk assessment) or (ii) if there is a lack of data, time, or resources for a quantitative microbial risk assessment. ( |
| Risk-benefit analysis | RBA | Frameworks that allow for quantitative comparison of benefits and risks associated with an action, typically in a local system. RBA can also be expanded to account for global (e.g., beyond the system) benefits and risks ( |
| Trade-off risk assessment | NA1 | A tool that can be used for RBA. Trade-off risk assessments use a risk assessment framework to compare competing solutions to a risk management issue within a system by accounting for both local (i.e., within the system) and global (i.e., beyond the system) benefits and risks, including social, economic, and environmental benefits and risks. |
Description of terms relevant for trade-off risk assessments.
1NA, not applicable.
Summary
Keywords
artificial intelligence, food safety, microbial, predictive modeling, public health, risk assessments, sustainability, trade-offs
Citation
Wiedmann M, Sunil S, Moreno-Switt AI, Vongkamjan K and Johler S (2026) Balancing food safety and sustainability: trade-off risk assessments and predictive modeling. Front Sci 4:1720772. doi: 10.3389/fsci.2026.1720772
Received
08 October 2025
Revised
06 January 2026
Accepted
18 February 2026
Published
17 March 2026
Volume
4 - 2026
Edited by
Chris Elliott, Queen’s University Belfast, United Kingdom
Reviewed by
Mieke Uyttendaele, Ghent University, Belgium
Lee-Ann Jaykus, North Carolina State University, United States
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© 2026 Wiedmann, Sunil, Moreno-Switt, Vongkamjan and Johler.
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*Correspondence: Martin Wiedmann, mw16@cornell.edu
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