Recalls / Active ingredient / Misoprostol

Misoprostol

7 FDA drug recalls involving the active ingredient “Misoprostol”.

Date	Class	Product	Firm
2016-09-09	Class III	Cytotec (misoprostol) Tablets, 200 mcg, 100 Tablets blister pack (10X10), For in-institution use only, Rx only	Pfizer Inc.
2014-09-26	Class II	Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75 mg/0.2 mg, 60-count bottle, Rx only. Manufacture	Actavis Laboratories, FL, Inc.
2014-04-24	Class II	Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 50 mg/0.2 mg, 60-count bottle, Rx only, Manufacture	Actavis Laboratories, FL, Inc.
2014-04-24	Class II	Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75 mg/0.2 mg, 60-count bottle, Rx only, Manufacture	Actavis Laboratories, FL, Inc.
2013-12-20	Class II	Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75 mg/0.2 mg, 60-count bottle, Rx only, Manufacture	Watson Laboratories, Inc.-(Actavis) - Florida
2013-03-22	Class II	Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg, 60-count bottle, Rx only, Manufactured	Watson Laboratories, Inc.-(Actavis) - Florida
2013-03-22	Class II	Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg, Rx only, Manufactured by Watson Laborat	Actavis Inc