Actavis Inc Recall: Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg,
Actavis Inc Recall: Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg, is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Actavis Inc; Product: Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg, Rx only, Manufactured by Watson Laboratories, Inc., Co
| Recalling firm | Actavis Inc |
|---|---|
| Product | Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg, Rx only, Manufactured by Watson Laboratories, Inc., Corona, CA 92880, NDC 0591-0398-60 (60 count bottles) |
| Reason for recall | Failed Tablet/Capsule Specifications: Broken tablets |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Nationwide |
| Recall initiated | 20130322 |
| Recall number | D-1060-2014 |
| Category | drug |
| State | NJ |
| Country | United States |
$29/mo
Try RecallGuard →