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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

Apotex Corp.: CGMP Deviations: Apotex Corporation, Weston, FL is recalling multiple products in the US market manufactured prior to August 2009 using API and raw materials that had passed the vendor's suggested expiry. Products include Benazepril HCL 5mg, Citalopram FCT 40mg, Diltiazem XR 180mg & 240mg, Gemfibrozil 600mg, Loratadine 10mg, Lovastatin 20mg, 20mg, & 40mg, Nizatidine 150mg & 300mg, and Terazosin H; CGMP Deviations: Apotex Corporation, Weston, FL is recalling multiple products in th

Agency Publication Date: September 22, 2010
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 56733
Status: Resolved
Manufacturer: Apotex Corp.
Manufactured In: United States
Units Affected: 12 products (12,839 bottles; 27,932 bottles; 17,908 bottles; 13,238 bottles; 7,777 bottles; 57,243 bottles; 3,096 bottles; 22,368 bottles; 14,153 bottles; 19,136 bottles; 2,188 bottles; 20,193 bottles)

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.