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A Food Safety News publisher says seven petitions have been filed or prepared for the FDA and USDA’s Food Safety and Inspection Service, seeking changes to food testing, consumer warnings and outbreak investigations. The proposals address infant formula, raw-milk cheese, sprouts, poultry, animal-feeding operations and the naming of firms implicated in outbreaks; the source does not provide agency responses or decisions.
A Food Safety News publisher has outlined seven petitions directed to the FDA and USDA’s Food Safety and Inspection Service, seeking new or formalized steps on food testing, warning labels, outbreak sampling and disclosure. The proposals span infant formula, raw-milk cheese, sprouts and poultry, and call for clearer access to outbreak-related information; the report does not say the agencies have accepted or acted on them.
The petitions described in the publisher’s platform include requests for FDA to add botulinum neurotoxin-producing clostridia to required finished-product testing for powdered infant formula and to require testing of dairy ingredients used to make it. The author says 52 infants have been hospitalized with botulism in the ByHeart and Nara Organics outbreaks since 2023, and says the organism was found in a dairy ingredient. The petition is being brought with 46 parents representing 24 infants, according to the report.
Two other FDA proposals focus on consumer warnings. One asks for a prescribed label on cheese made with raw milk, alongside completion of the agency’s review of the 60-day aging rule and a requirement that cheesemakers validate aging as a safety measure. Another would require warnings on packaged raw and lightly cooked sprouts, including sprouts sold in salads, sandwiches and wraps. The author says FDA has advised higher-risk groups against eating raw sprouts for decades, but that advice has not appeared on product packaging.
A petition to USDA’s FSIS asks the agency to classify Salmonella at or above 1 CFU per gram as an adulterant in raw ground chicken and turkey and raw chicken parts. As alternatives, it proposes applying the designation to three Salmonella serotypes or beginning verification sampling that the agency had announced and later postponed, according to the report. The remaining petitions seek limited FDA sampling access to animal-feeding operations implicated in multistate outbreaks and a written disclosure standard for firms implicated by outbreak evidence. The source lists seven petitions but its supplied text ends during the final disclosure proposal, so details of the seventh are incomplete.
Changes Across the Food-Safety Chain
The requests could affect how regulators detect hazards before products reach consumers and what information is available during an outbreak. Testing requirements would apply at production stages, while warning labels would put agency advice directly in front of shoppers choosing foods that can carry pathogens. The proposals are requests, not adopted rules, so they do not change current requirements on their own.
The petitions also address the information and evidence available to investigators. The author argues that limited access to implicated animal operations can constrain environmental sampling, and that withholding firm identities can leave consumers without a clear way to identify products involved in an investigation. Any action would depend on agency review, statutory authority and the evidence supporting each request.
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Earlier Rules and Agency Decisions
The report links several requests to existing or prior agency actions. Federal rules already require finished powdered infant formula testing for Cronobacter and Salmonella, according to the author, while the proposed petition would add another organism. The raw-cheese proposal challenges reliance on a 60-day aging rule dating to the 1940s; the author says FDA announced a reevaluation in 2013 but has not completed it.
For poultry, the author points to an FSIS determination in May 2024 that Salmonella at or above 1 CFU per gram is an adulterant in breaded stuffed raw chicken products. The report says a broader proceeding for other raw poultry was withdrawn in April 2025 and that announced verification sampling was postponed indefinitely in December 2025. On disclosure, it cites FDA outbreak announcements in which the agency identified foods but did not name firms, while arguing that the agency has named firms in other cases. These are the petitioner’s account of the regulatory record.
““No seizures, no husbandry rules, no financial records. Just samples.””
— The petition author, describing the animal-feeding-operation proposal
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Petition Status and Agency Response
The supplied report does not establish whether all seven petitions have been formally filed, when each was submitted, or whether FDA and FSIS have acknowledged them. It gives no agency response, review schedule or decision timeline. The source text also cuts off during the final proposal, leaving the full scope and wording of that petition—and the complete description of the seventh request—unclear.
The outbreak figures and descriptions are presented by the petition author; the supplied material does not include independent agency statements or supporting records for each assertion. It is also unclear whether either agency will grant, reject or modify any requested measure, or whether the proposals would proceed through rulemaking or another process.
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Agency Review and Filing Details
The next confirmed milestones would be publication or confirmation of the petitions’ filing, followed by any response from FDA or FSIS. The report provides no dates for those steps. If agencies decide to pursue changes requiring regulation, they may need to set out proposed requirements and allow public comment; the source does not say whether that process has begun.
Readers should look for the complete petition texts and agency records to verify the precise requests, filing dates and legal arguments. Until an agency acts, the listed measures remain proposals, not new food-safety rules.
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Key Questions
What are the seven petitions asking federal agencies to do?
They seek stronger testing for powdered infant formula and poultry, warning labels for raw-milk cheese and sprouts, limited sampling access to animal-feeding operations implicated in outbreaks, and a written standard for disclosing firms implicated by outbreak evidence. The source material provided does not fully describe the seventh petition.
Have FDA or USDA adopted these proposals?
No adoption is reported. The petitions are requests to the FDA and USDA’s Food Safety and Inspection Service. The source gives no agency decision or response.
What changes are proposed for powdered infant formula?
The petition asks FDA to add botulinum neurotoxin-producing clostridia to the organisms tested in finished powdered formula and to require testing of dairy ingredients used in production.
Would the proposals immediately change food labels or testing rules?
No. A petition does not itself change requirements. FDA or FSIS would need to review the requests and take further action before any new rules or labeling requirements applied.
What remains unknown about the petitions?
The report does not give complete filing details, agency responses or review timelines. Its supplied text also ends before the final disclosure proposal is fully described and does not clearly identify the seventh petition.
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