Hospira Inc. Recall: Diazepam Injection, USP, 5 mg/mL, 10 mL, Multiple-dose Sterile Non-py
Hospira Inc. Recall: Diazepam Injection, USP, 5 mg/mL, 10 mL, Multiple-dose Sterile Non-py is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Hospira Inc.; Product: Diazepam Injection, USP, 5 mg/mL, 10 mL, Multiple-dose Sterile Non-pyrogenic, Fliptop Vial, C-IV, Rx Only, Hospira, Inc., La
| Recalling firm | Hospira Inc. |
|---|---|
| Product | 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 |
| Reason for recall | Lack of assurance of sterility: ineffective crimp on fliptop vials that may result in leaking at the neck of the vials. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Nationwide and Puerto Rico |
| Recall initiated | 20130816 |
| Recall number | D-927-2013 |
| Category | drug |
| State | IL |
| Country | United States |
$29/mo
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