Drug recall
Diazepam Injection, USP, 5 mg/mL, 10 mL, Multiple-dose Sterile Non-pyrogenic, Fliptop Vial, C-IV, Rx Only…
FDA recall event 66104 · Class II · Hospira Inc.
Key facts
| Event ID | 66104 |
|---|---|
| Recall numbers | D-927-2013 |
| Recalling firm | Hospira Inc. |
| Product type | Drugs |
| Products | Diazepam Injection, USP, 5 mg/mL, 10 mL, Multiple-dose Sterile Non-pyrogenic, Fliptop Vial, C-IV, Rx Only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-3213-12 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Lack of assurance of sterility: ineffective crimp on fliptop vials that may result in leaking at the neck of the vials. |
| Initiation date | Aug 16, 2013 |
| Report date | Sep 4, 2013 |
| Termination date | Oct 28, 2014 |
| 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 · Source date: