Drug recall
Intravenous Sodium Edecrin (Ethacrynate Sodium) 50 mg single use vial, Rx only, Dist by: Merck & Co., Inc…
FDA recall event 31644 · Class II · Merck & Co Inc, Merck Manufacture
Key facts
| Event ID | 31644 |
|---|---|
| Recall numbers | D-223-5 |
| Recalling firm | Merck & Co Inc, Merck Manufacture |
| Product type | Drugs |
| Products | Intravenous Sodium Edecrin (Ethacrynate Sodium) 50 mg single use vial, Rx only, Dist by: Merck & Co., Inc. West Point, PA 19486 USA, NDC 0006-3620-50 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Subpotent |
| Initiation date | Apr 11, 2005 |
| City | West Point |
| Country | United States |
| FEI number | 2510592 |
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