Actavis Laboratories, FL, Inc. recalls Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75 mg/0.2 mg, 60-count bottle, Rx only, Manufactured by: Wats
Recalled October 8, 2014 · FDA recall D-1616-2014 · Actavis Laboratories, FL
Hazard
Failed Tablet/Capsule Specifications: Recall due to complaints of split or broken tablets. · FDA Class II
Units
36,538 bottles
Sold at
Nationwide and Puerto Rico
Description
Failed Tablet/Capsule Specifications: Recall due to complaints of split or broken tablets.
Product
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.
Manufacturer(s)
Actavis Laboratories, FL, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →