Drug recall
Dexium 0.25 mg Dexamethasone Tablets in bottles of 1000 tablets per bottle
FDA recall event 28418 · Class III · Bimeda, Inc.
Key facts
| Event ID | 28418 |
|---|---|
| Recall numbers | V-124-4 |
| Recalling firm | Bimeda, Inc. |
| Product type | Veterinary |
| Products | Dexium 0.25 mg Dexamethasone Tablets in bottles of 1000 tablets per bottle |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failure to meet USP dissolution requirements during product stability testing. |
| Initiation date | Feb 24, 2004 |
| City | Le Sueur |
| Country | United States |
| FEI number | 2110168 |
At a glance
- 1–9 Products in this recall
- 10–99 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