Hospira Inc. Recall: Lidocaine HCl Injection, USP, 2%, 20 mg per mL, Preservative-Free, 5
Hospira Inc. Recall: Lidocaine HCl Injection, USP, 2%, 20 mg per mL, Preservative-Free, 5 is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Hospira Inc.; Product: Lidocaine HCl Injection, USP, 2%, 20 mg per mL, Preservative-Free, 5 mL Single-Dose Vial, Rx only, For Infiltration and Nerve
| Recalling firm | Hospira Inc. |
|---|---|
| Product | Lidocaine HCl Injection, USP, 2%, 20 mg per mL, Preservative-Free, 5 mL Single-Dose Vial, Rx only, For Infiltration and Nerve Block including Epidural and Caudal, Manufactured by: Hospira, Inc., Lake Forest, IL, 60045, NDC 0409-2066-05 |
| Reason for recall | Presence of Particulate Matter: The product was discolored and contained visible particulates (iron oxide) in the solution and embedded in the glass vial. |
| Classification | Class I (most serious — reasonable probability of serious health consequences or death) |
| Status | Terminated |
| Distribution | Nationwide |
| Recall initiated | 20140729 |
| Recall number | D-0020-2015 |
| Category | drug |
| State | IL |
| Country | United States |
$29/mo
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