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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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