Hospira Inc. Recall: Furosemide Injection, USP, 40 mg/4mL (10 mg/mL), 4 ml Single-Dose Via
Hospira Inc. Recall: Furosemide Injection, USP, 40 mg/4mL (10 mg/mL), 4 ml Single-Dose Via is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Hospira Inc.; Product: Furosemide Injection, USP, 40 mg/4mL (10 mg/mL), 4 ml Single-Dose Vial, Rx only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA, ND
| Recalling firm | Hospira Inc. |
|---|---|
| Product | Furosemide Injection, USP, 40 mg/4mL (10 mg/mL), 4 ml Single-Dose Vial, Rx only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA, NDC 0409-6102-04 |
| Reason for recall | Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Nationwide and Puerto Rico |
| Recall initiated | 20130226 |
| Recall number | D-314-2013 |
| Category | drug |
| State | IL |
| Country | United States |
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