Diclofenac Sodium and Misoprostol Delayed-Release recall
Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75 mg/0.2 mg, 60-count bottle, Rx only, Manufactured by: Watson Laboratories, Inc., Corona…
Why was Diclofenac Sodium and Misoprostol Delayed-Release recalled?
Failed Tablet/Capsule Specifications: Split tablets were found in the 12-month stability samples.
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# 605957A, Exp 09/14
- Product
- Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75 mg/0.2 mg, 60-count bottle, Rx only, Manufactured by: Watson Laboratories, Inc., Corona…
- Recalling firm
- Watson Laboratories, Inc.-(Actavis) - Florida
- Quantity
- 5987 bottles
- Distribution
- Nationwide
- Recall date
- February 19, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)