Hospira Inc. Recall: Potassium Chloride for Inj. Concentrate, USP, 40 mEq (2 mEq/mL), 20 m
Hospira Inc. Recall: Potassium Chloride for Inj. Concentrate, USP, 40 mEq (2 mEq/mL), 20 m is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Hospira Inc.; Product: Potassium Chloride for Inj. Concentrate, USP, 40 mEq (2 mEq/mL), 20 mL Single-dose Fliptop Vial, For IV use, Rx only, Hospir
| Recalling firm | Hospira Inc. |
|---|---|
| Product | Potassium Chloride for Inj. Concentrate, USP, 40 mEq (2 mEq/mL), 20 mL Single-dose Fliptop Vial, For IV use, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA |
| Reason for recall | Presence of Particulate; red and black particulate within the solution and embedded within the plastic vial identified as iron oxide |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Nationwide |
| Recall initiated | 20140327 |
| Recall number | D-1261-2014 |
| Category | drug |
| State | IL |
| Country | United States |
$29/mo
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