Hospira Inc. Recall: Sodium Chloride Injection, USP, 0.9%, 20 mL Single-dose Fliptop Plast
Hospira Inc. Recall: Sodium Chloride Injection, USP, 0.9%, 20 mL Single-dose Fliptop Plast is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Hospira Inc.; Product: Sodium Chloride Injection, USP, 0.9%, 20 mL Single-dose Fliptop Plastic Vial, packaged in 25 vial Units per carton, Rx only,
| Recalling firm | Hospira Inc. |
|---|---|
| Product | Sodium Chloride Injection, USP, 0.9%, 20 mL Single-dose Fliptop Plastic Vial, packaged in 25 vial Units per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-4888-20. |
| Reason for recall | Presence of Particulate Matter: Confirmed customer report of visible particulate in the form of an orange or rust colored ring embedded in between the plastic layers of the plastic vial. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Nationwide and Guam |
| Recall initiated | 20130627 |
| Recall number | D-813-2013 |
| Category | drug |
| State | IL |
| Country | United States |
$29/mo
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