Drug recall
Diazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only, Hospira Inc. Lake Forest, IL 60045, NDC 0409-1273-32
FDA recall event 74399 · Class II · Hospira Inc.
Key facts
| Event ID | 74399 |
|---|---|
| Recall numbers | D-1359-2016 |
| Recalling firm | Hospira Inc. |
| Product type | Drugs |
| Products | Diazepam Injection USP 10mg/2mL (5 mg/mL, 2 mL), Rx only, Hospira Inc. Lake Forest, IL 60045, NDC 0409-1273-32 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Crystallization: Product contains particulate identified to be crystallized active ingredient. |
| Initiation date | Jun 23, 2016 |
| Report date | Jul 20, 2016 |
| Termination date | Aug 31, 2018 |
| 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: