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 Laboratories, FL, Inc. Due to Failed Tablet/Capsule Specifications: Recall due to complaints of...
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 Laboratories, FL, Inc. directly.
Affected Products
Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75 mg/0.2 mg, 60-count bottle, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA 92880, NDC 0591-0398-60, UPC 3 05910 39860 6.
Quantity: 36,538 bottles
Why Was This Recalled?
Failed Tablet/Capsule Specifications: Recall due to complaints of split or broken tablets.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Actavis Laboratories, FL, Inc.
Actavis Laboratories, FL, Inc. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report