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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 Scientific, Inc: Failed Dissolution Specification: Out of specification dissolution results when testing product stability.

Agency Publication Date: July 14, 2016
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Affected Products

Product: Duloxetine Delayed-Release Capsules, USP, 20 mg, 60-count bottles, Rx only, Manufactured by Apotex Inc, Toronto, Ontario M9L 1T9, Manufactured for Apotex Corp. Weston Florida 33326, NDC 60505-2995-6; UPC # 360505299560;

Lot #: KV9795, KV9794, KV9796, KX6278; Exp 04/30/2016.

Lot Numbers:
KV9795
Product: Duloxetine Delayed-Release Capsules, USP, 60 mg, 30-count bottles, Rx only, Manufactured by Apotex Inc, Toronto, Ontario M9L 1T9, Manufactured for Apotex Corp. Weston Florida 33326, NDC 60505-2997-3; UPC # 360505299737;

Lot #: KW2167,KY9960, KV9789, KV9788; Exp 02/29/2016; Lot #: KY9961, Exp 04/30/2016; Lot #: KX6311, KX6312, KY7795, KX6315, Exp 05/31/2016; Lot #: KX6317, Exp 06/30/2016.

Lot Numbers:
KW2167
KY9961
KX6311
KX6317
Product: Duloxetine Delayed-Release Capsules, USP, 30 mg, 30-count bottles, Rx only, Manufactured by Apotex Inc, Toronto, Ontario M9L 1T9, Manufactured for Apotex Corp. Weston Florida 33326, NDC 60505-2996-3; UPC # 360505299638.

Lot #: KY5120, KW2164, KY9953, KV9791, KV9792, Exp 03/31/2016.

Lot Numbers:
KY5120

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 73419
Status: Resolved
Manufacturer: Apotex Scientific, Inc
Manufactured In: United States
Units Affected: 3 products (107,880 (60 ct bottle); 605,989 (30 ct) bottles; 750,273 (30 ct) 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.