August Food and Agriculture Regulatory Recap

OFW’s Food & Agriculture team regularly monitors announcements and policy issuances from FDA, USDA, and other agencies to keep our clients apprised of regulatory developments that may impact their business. Here are a few of the developments from August that should be highlighted. If you have any questions or would like more information, please do not hesitate to reach out to us.


U.S. Food and Drug Administration (FDA)

  • On August 9, 2023, FDA published a direct final rule, “Revocation of Uses of Partially Hydrogenated Oils (PHOs) in Foods, which completes the agency’s June 17, 2015, final determination that PHOs in food are no longer Generally Recognized As Safe (GRAS). Simultaneously, FDA issued a companion proposed rule that would revoke the use of PHOs. FDA published the proposed rule as a fallback measure in case the direct final is withdrawn (due to the submission of significant adverse comments).

  • On August 23, 2023, FDA announced the selection of James “Jim” Jones to serve as the first Deputy Commissioner for Human Foods. The Deputy Commissioner role was established as part of FDA’s recent proposal to reorganize the Human Food Program.

United States Department of Agriculture (USDA)

  • On August 17, 2023, USDA’s Food Safety and Inspection Service (FSIS) published the final rule, “Condemnation of Poultry Carcasses Affected with any Form of Avian Leukosis Complex; Recession.” The final rule officially amends the Poultry Products Inspection Act (PPIA) regulations to rescind several regulations requiring the condemnation of poultry carcasses affected with any form of avian leukosis complex (avian leukosis). Beginning September 18th, avian leukosis will be a “trimmable” condition.

Other  

  • On August 30, 2023, The National Advisory Committee on Microbiological Criteria for Foods (NACMCF) – an advisory committee originally established in 1988 by USDA – hosted a subcommittee Plenary Public Meeting. The 2021-2023 current NACMCF subcommittee work can be found here.  During the meeting, NACMCF focused on two FDA subcommittee charges:
    • Cyclospora cayetanensis in Produce – The subcommittee discussed, voted, and officially adopted the report and recommendations on C. cayetanensis in produce. The draft report and recommendations can be found here. The final report will be posted here shortly.

    • Cronobacter Spp. in Powdered Infant Formula – The subcommittee provided an update on the charge related to Cronobacter spp. in powdered infant formula.

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Please contact Kyla Kaplan (kkaplan@ofwlaw.com) if you have any questions or are interested in additional assistance.

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