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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

Allscripts LLC: Allscripts repackaged products being recalled by the manufacturer, Able Laboratories, due to a lack of assurance that testing conducted for release and stability conformed to standard operating procedures.

Agency Publication Date: July 8, 2005
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 32266
Status: Active
Manufacturer: Allscripts LLC
Manufactured In: United States
Units Affected: 8 products (10,828 capsules; 48,134 tablets; 8,808 suppositories; 17,372 tablets; 158,832 tablets; 3,168 suppositories; 1,848 tablets; 54,270 tablets)

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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.