Hospira Inc. Recall: 0.9% Sodium Chloride Injection, USP, a) 50 mL (NDC 0409-7984-13), b)
Hospira Inc. Recall: 0.9% Sodium Chloride Injection, USP, a) 50 mL (NDC 0409-7984-13), b) is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Hospira Inc.; Product: 0.9% Sodium Chloride Injection, USP, a) 50 mL (NDC 0409-7984-13), b) 50 mL (NDC 0409-7984-36), c) 100 mL (0409-7984-37), Rx O
| Recalling firm | Hospira Inc. |
|---|---|
| Product | 0.9% Sodium Chloride Injection, USP, a) 50 mL (NDC 0409-7984-13), b) 50 mL (NDC 0409-7984-36), c) 100 mL (0409-7984-37), Rx Only, Hospira, Inc., Lake Forest, IL 60045 |
| Reason for recall | Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Nationwide Puerto Rico, U.S. Virgin Island, Libya, Saudi Arabia |
| Recall initiated | 20120504 |
| Recall number | D-619-2013 |
| Category | drug |
| State | IL |
| Country | United States |
$29/mo
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