Diclofenac Sodium AND Misoprostol: 6 recalls on record

Recalled by 1 agency: FDA (6).

First recall on record: July 31, 2013. Most recent: December 3, 2014.

Risk classification: Class II: 6

Most recent recalls

DateAgencyProduct
December 3, 2014FDADiclofenac Sodium and Misoprostol Delayed-Release Tablets, 75 mg/0.2 mg, 60-count bottle,…D-0258-2015
October 8, 2014FDADiclofenac Sodium and Misoprostol Delayed-Release Tablets, 50 mg/0.2 mg, 60-count bottle,…D-1617-2014
October 8, 2014FDADiclofenac Sodium and Misoprostol Delayed-Release Tablets, 75 mg/0.2 mg, 60-count bottle,…D-1616-2014
February 19, 2014FDADiclofenac Sodium and Misoprostol Delayed-Release Tablets, 75 mg/0.2 mg, 60-count bottle,…D-1082-2014
February 12, 2014FDADiclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg, Rx only, Manufactu…D-1060-2014
July 31, 2013FDADiclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg, 60-count bottle, R…D-817-2013

Questions about this brand

How many recalls does Diclofenac Sodium AND Misoprostol have?
Recalert has 6 U.S. recalls on record for Diclofenac Sodium AND Misoprostol, published between July 31, 2013 and December 3, 2014.
What was the most recent Diclofenac Sodium AND Misoprostol recall?
FDA recall D-0258-2015, published December 3, 2014: 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.
Which agencies have recalled Diclofenac Sodium AND Misoprostol products?
Diclofenac Sodium AND Misoprostol products appear in recalls from: FDA (6).

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