Drug recall
Methocarbamol Tablets USP, 500 mg, 100 and 500 tablet bottles, WATSON, Rx Only, Watson Laboratories, Inc…
FDA recall event 25962 · Class III · Watson Pharmaceuticals Inc
Key facts
| Event ID | 25962 |
|---|---|
| Recall numbers | D-240-3 |
| Recalling firm | Watson Pharmaceuticals Inc |
| Product type | Drugs |
| Products | Methocarbamol Tablets USP, 500 mg, 100 and 500 tablet bottles, WATSON, Rx Only, Watson Laboratories, Inc., Corona, CA 92880. NDC #0591-5381-01(100''s)//NDC #0591-5381-05 (500''s) |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Dissolution Failure; 3 month stability sample |
| Initiation date | Apr 15, 2003 |
| City | Corona |
| Country | United States |
| FEI number | 3003944123 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports