Drug recall
Diazepam Injection, USP, 5 mg/mL, 10 mL Multiple Dose Fliptop Vials, 10 Units per carton, Rx only, Hospira…
FDA recall event 59447 · Class III · Hospira Inc.
Key facts
| Event ID | 59447 |
|---|---|
| Recall numbers | D-772-2011 |
| Recalling firm | Hospira Inc. |
| Product type | Drugs |
| Products | Diazepam Injection, USP, 5 mg/mL, 10 mL Multiple Dose Fliptop Vials, 10 Units per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA; NDC 0409-3213-12 |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | CGMP Deviations: this lot was inadvertently release when it should have been destroyed, the product met all specifications at time of release. |
| Initiation date | Jun 6, 2011 |
| Termination date | Nov 18, 2011 |
| City | Lake Forest |
| State | IL |
| Country | United States |
| FEI number | 3005579246 |
At a glance
- 1–9 Products in this recall
- None 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