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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

Alpharma USPD: Product lacks assurance it meets microbial release specification; Product failed water content specification; Subpotency at in-processing stage of manufacturing; Viscosity failure and incorrect mixing speeds used during manufacturing; Manufacturing Deviation; Excessive product hold time prior to filling; Product lacks complete manufacturing validation

Agency Publication Date: January 17, 2003
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 25049
Status: Resolved
Manufacturer: Alpharma USPD
Manufactured In: United States
Units Affected: 18 products (137358 units; 52296 units; 2856 units; 25174 units; 38544 units; 77803 units; 77803 units; 93432 units; 38952 units; 23592 units; 384231 units; 33732 units; 536,160 units; 68,712 units; 83,468 units; 44,045 units; 144,156 units; 26,614 units)

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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.