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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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Medium RiskFDA Drug

Wyeth Ayerst Laboratories: Lack of Assurance of Sterility; possible damage to the breakaway cap

Agency Publication Date: July 14, 2006
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 35523
Status: Resolved
Manufacturer: Wyeth Ayerst Laboratories
Manufactured In: United States
Units Affected: 3 products (62,465 vials and 5,129 vials; 272,510 vials and 31,274 vials; 50,378 vials and 5,325 vials)

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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.