Watson Laboratories Inc Recall: Oxycodone and Acetaminophen Capsules, USP 5mg/500 mg, pack
Watson Laboratories Inc Recall: Oxycodone and Acetaminophen Capsules, USP 5mg/500 mg, pack is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Watson Laboratories Inc; Product: Oxycodone and Acetaminophen Capsules, USP 5mg/500 mg, packaged in a)100-count bottle (NDC 0591-0737-01), b) 500-c
| Recalling firm | Watson Laboratories Inc |
|---|---|
| Product | Oxycodone and Acetaminophen Capsules, USP 5mg/500 mg, packaged in a)100-count bottle (NDC 0591-0737-01), b) 500-count bottle (NDC 0591-0737-05), Rx only, Manufactured by Watson Laboratories, Inc., Corona, CA92880. |
| Reason for recall | Subpotent drug: Two lots of Oxycodone and Acetaminophen Capsules, USP 5/500 mg are being recalled due to low out of specification (OOS) assay result obtained at expiry (24 months) for the oxycodone portion of the product. |
| Classification | Class III (least serious — unlikely to cause adverse health consequences) |
| Status | Terminated |
| Distribution | Nationwide |
| Recall initiated | 20130719 |
| Recall number | D-823-2013 |
| Category | drug |
| State | CA |
| Country | United States |
$29/mo
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