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 Actavis Inc 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 Actavis Inc directly.
Affected Products
Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg, Rx only, Manufactured by Watson Laboratories, Inc., Corona, CA 92880, NDC 0591-0398-60 (60 count bottles)
Quantity: 6,540 bottles
Why Was This Recalled?
Failed Tablet/Capsule Specifications: Broken tablets
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Actavis Inc
Actavis Inc has 17 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report