Drug recall
Ciprofloxacin Injection, USP, 400 mg, 40 mL single dose vial, Rx only, Hospira, Inc., Lake Forest, IL 60045…
FDA recall event 52699 · Class III · Hospira, Inc.
Key facts
| Event ID | 52699 |
|---|---|
| Recall numbers | D-1893-2009 |
| Recalling firm | Hospira, Inc. |
| Product type | Drugs |
| Products | Ciprofloxacin Injection, USP, 400 mg, 40 mL single dose vial, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA --- NDC 0409-4778-86, |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Discoloration |
| Initiation date | Jun 24, 2009 |
| Termination date | Mar 31, 2011 |
| City | Lake Forest |
| State | IL |
| Country | United States |
| FEI number | 3003940565 |
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