Hospira Inc. Recall: 0.9% Sodium Chloride Injection, USP, 50 mL, Manufactured by Hospira,
Hospira Inc. Recall: 0.9% Sodium Chloride Injection, USP, 50 mL, Manufactured by Hospira, is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Hospira Inc.; Product: 0.9% Sodium Chloride Injection, USP, 50 mL, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7984-36 Hospira, I
| Recalling firm | Hospira Inc. |
|---|---|
| Product | 0.9% Sodium Chloride Injection, USP, 50 mL, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7984-36 Hospira, Inc., Lake Forest, IL 60045 |
| Reason for recall | Lack of Assurance of Sterility: The product is being recall due to the product lot being incorrectly released without meeting product specifications. There is the potential for the solution to leak from the administrative port to the fill tube seal. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Nationwide |
| Recall initiated | 20130218 |
| Recall number | D-243-2013 |
| Category | drug |
| State | IL |
| Country | United States |
$29/mo
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