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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

American Pharmaceutical Partners, Inc.: Stability; lack of assurance that product potency will be maintained through labeled expiration

Agency Publication Date: July 20, 2004
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 29036
Status: Active
Manufacturer: American Pharmaceutical Partners, Inc.
Manufactured In: United States
Units Affected: 12 products (607,073 vials; 62,725 vials; 22,575 vials; 71,850 vials; 165,100 vials; 178,390 vials; 21,025 vials; 20,525 vials; 208,300 vials; 41,175 vials; 82,800 vials; 406,300 vials)

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.