PlainRecalls
FDA Drug Moderate Class II Terminated

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)

Reported: February 12, 2014 Initiated: March 22, 2013 #D-1060-2014

Product Description

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)

Reason for Recall

Failed Tablet/Capsule Specifications: Broken tablets

Details

Recalling Firm
Actavis Inc
Units Affected
6,540 bottles
Distribution
Nationwide
Location
Parsippany, NJ

Frequently Asked Questions

What product was recalled?
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). Recalled by Actavis Inc. Units affected: 6,540 bottles.
Why was this product recalled?
Failed Tablet/Capsule Specifications: Broken tablets
Which agency issued this recall?
This recall was issued by the FDA Drug on February 12, 2014. Severity: Moderate. Recall number: D-1060-2014.