FDAFDA · Food and drugs·Recall number D-0258-2015
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 December 3, 2014 · Recall initiated: September 26, 2014
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: Presence of split or broken tablets.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- DICLOFENAC SODIUM AND MISOPROSTOL
- Manufacturer
- Actavis Laboratories, FL, Inc.
- Distributor
- U.S. Nationwide including Puerto Rico.
- UPC
- 305910398606
- Lot
- Lot # 694320A, Expiry: 02/28/2015.
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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