FDAClass IIFebruary 12, 2014

Diclofenac Sodium and Misoprostol Delayed-Release recall

Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg, Rx only, Manufactured by Watson Laboratories, Inc., Corona, CA 92880, NDC…

Why was Diclofenac Sodium and Misoprostol Delayed-Release recalled?

Failed Tablet/Capsule Specifications: Broken tablets

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot 668271A, Exp 11/14 and Lot 684119A Exp 01/2015

Product
Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg, Rx only, Manufactured by Watson Laboratories, Inc., Corona, CA 92880, NDC…
Recalling firm
Actavis Inc
Quantity
6,540 bottles
Distribution
Nationwide
Recall date
February 12, 2014
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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