Recall: D-1617-2014

Class II - Potentially Harmful

Class IIClassification

2014-04-24Initiated

TerminatedStatus

Actavis Laboratories, FL, Inc.Firm

Product

Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 50 mg/0.2 mg, 60-count bottle, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA 92880, NDC 0591-0397-60, UPC 3 05910 39760 9.

Reason

Failed Tablet/Capsule Specifications: Recall due to complaints of split or broken tablets.

Distribution

Nationwide and Puerto Rico

Source: FDA drug enforcement report via openFDA (Voluntary: Firm initiated). If you take this product, talk to your pharmacist or doctor before stopping it.