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FDA Issues Final Guidance for Voluntary Recalls

By Emily Lyons on March 14, 2022
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Earlier this month, the U.S. Food and Drug Administration (“FDA”) completed guidance to help companies remove violative products from the market in a swift and effective manner. The guidance describes the precautionary steps companies should take to develop recall policies and procedures that include training, planning, and recordkeeping to reduce the amount of time a recalled product is exposed to the public.

The FDA’s final guidance explains a variety of best practices for establishing, implementing and training on a recall plan. Some recommendations include:

  • Using an adequate product coding and maintain distribution records to facilitate quicker, and more accurate recall actions.
  • Developing recall procedures to swiftly inform their entire distribution chain of the recall, thus, consignees can rapidly identify affected lots and recall downstream products when necessary.
  • Using electronic communications to quickly identify and provide certain product detail when alerting consignees and the public about a voluntary recall.
  • Acting quickly to initiate a recall when the public’s health is at risk prior to completing an investigation into the cause of the recall.

Over the past several years, FDA has issued a variety of guidance documents to made proactive and systemic improvements to the recall process. These guidance documents include the following topics:

  • Public availability of lists of retail consignees to effectuate certain human and animal food recalls;
  • Mandatory recalls for human and animal foods; and
  • Public warnings and notifications for all FDA-regulated products, which reiterates a policy to rapidly post new recalls to the FDA’s weekly Enforcement Reports, a public listing of all recalls monitored by the FDA.

The FDA’s guidance reflects the agency’s ongoing commitment to work closely with companies so they can quickly act to protect the public from violative products on the market. Food, dietary supplement, medical device, and cosmetic industry members are encouraged to reach out to their Husch Blackwell attorney or a member of the Food & Agribusiness team, to discuss how their current recall plans should be updated in light of this guidance or how to establish a recall plan.

Written with the assistance of Sabrina Bey, a Fall Clerk in the Husch Blackwell LLP Washington, DC office.

Photo of Emily Lyons Emily Lyons

Emily grew up on a northern Illinois dairy farm, and now helps clients bridge the gap from farm to fork. She guides clients on complex regulatory issues as they bring dairy products, beverages, fruits and vegetables, processed foods and other agricultural goods to…

Emily grew up on a northern Illinois dairy farm, and now helps clients bridge the gap from farm to fork. She guides clients on complex regulatory issues as they bring dairy products, beverages, fruits and vegetables, processed foods and other agricultural goods to market. At the intersection of agriculture, food and environment, Emily handles compliance matters such as labeling, marketing, permitting and agency inquiries including the Food Safety Modernization Act, Pasteurized Milk Ordinance, USDA National Organic Program and bioengineered food disclosure standard, Generally Recognized as Safe status for food additives and food contact substances, and the Safe Drinking Water and Toxic Enforcement Act of 1986 (Proposition 65).

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  • Posted in:
    Food, Drug & Agriculture
  • Blog:
    Climate Solutions Legal Digest
  • Organization:
    Husch Blackwell LLP
  • Article: View Original Source

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