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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Drug

L. Perrigo Co.: Subpotency.

Agency Publication Date: June 29, 2011
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 59084
Status: Resolved
Manufacturer: L. Perrigo Co.
Manufactured In: United States
Units Affected: 8 products (288 boxes (864 Quit Tubes); 456 boxes (1,368 Quit Tubes); 1,920 boxes (5,760 Quit Tubes); 4,728 boxes (14,184 Quit Tubes); 264 boxes (792 Quit Tubes); 5,520 boxes (16,560 Quit Tubes); 528 boxes (1,584 Quit Tubes); 1,080 boxes (3,240 Quit Tubes))

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.