FDAFDA · Food and drugs·Recall number D-1082-2014
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.
Published February 19, 2014 · Recall initiated: December 20, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Tablet/Capsule Specifications: Split tablets were found in the 12-month stability samples.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Brand
- DICLOFENAC SODIUM AND MISOPROSTOL
- Manufacturer
- Watson Laboratories, Inc.-(Actavis) - Florida
- Distributor
- Nationwide
- UPC
- 305910398606
- Lot
- Lot# 605957A, Exp 09/14
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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