Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg, 60-count bottle, Rx only, Manufactured by Watson Laboratories, Inc., Corona, CA 92880, NDC 0591-0398-60
Class I - Dangerous 💊 Drugs
Recalled: March 22, 2013 Watson Laboratories, Inc.-(Actavis) - Florida Prescription Drugs
Nationwide
What Should You Do?
- Check if you have this product: Lot 635098A, Exp 10/14
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Watson Laboratories, Inc.-(Actavis) - Florida
- Reason for Recall:
- Failed Tablet/Capsule Specifications: Broken tablets
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg, 60-count bottle, Rx only, Manufactured by Watson Laboratories, Inc., Corona, CA 92880, NDC 0591-0398-60
Product Codes/Lot Numbers:
Lot 635098A, Exp 10/14
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: D-817-2013
Related Recalls
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.
Watson Laboratories, Inc.-(Actavis) - Florida
Class I - Dangerous
Failed Tablet/Capsule Specifications: Split tablets were found in the 12-month stability samples.