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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

Ferndale Laboratories, Inc.: Superpotent; pinhole defects in tubes may cause product to dry out and become more concentrated

Agency Publication Date: April 19, 2005
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 31449
Status: Active
Manufacturer: Ferndale Laboratories, Inc.
Manufactured In: United States
Units Affected: 4 products (27,459 tubes; 41,492 tubes; 13,570 tubes; 97,940 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.