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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 December 3, 2014 · FDA recall D-0258-2015 · Actavis Laboratories, FL

Hazard
Failed Tablet/Capsule Specifications: Presence of split or broken tablets. · FDA Class II
Units
5,451 Bottles
Sold at
U.S. Nationwide including Puerto Rico.

Description

Failed Tablet/Capsule Specifications: Presence 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

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 | RecallWatchUSA