Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by Watson Laboratories, Inc.-(Actavis) - Florida Due to Failed Tablet/Capsule Specifications: Broken tablets
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Watson Laboratories, Inc.-(Actavis) - Florida directly.
Affected Products
Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg, 60-count bottle, Rx only, Manufactured by Watson Laboratories, Inc., Corona, CA 92880, NDC 0591-0398-60
Quantity: 392,400 tablets
Why Was This Recalled?
Failed Tablet/Capsule Specifications: Broken tablets
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Watson Laboratories, Inc.-(Actavis) - Florida
Watson Laboratories, Inc.-(Actavis) - Florida has 2 total recalls tracked by RecallDetector.
Related Recalls
Icosapent Ethyl Capsules Recalled by Zydus Pharmaceuticals (USA) Inc Due to Failed Tablet/Capsule specifications: Red dots inside capsule and...
Zydus Pharmaceuticals (USA) Inc · March 9, 2026
Product label: Temozolomide Capsules Recalled by Rising Pharma Holding, Inc. Due to Failed Impurities/Degradation Specifications: An out-of-specification result observed during...
Rising Pharma Holding, Inc. · March 3, 2026
Semaglutide Inj. Recalled by New Life Pharma LLC Due to Lack of Assurance of Sterility
New Life Pharma LLC · February 26, 2026
Tirzepatide Inj Recalled by New Life Pharma LLC Due to Lack of Assurance of Sterility
New Life Pharma LLC · February 26, 2026
Tirzepatide Inj Recalled by New Life Pharma LLC Due to Lack of Assurance of Sterility
New Life Pharma LLC · February 26, 2026
Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report