Hospira Inc. recalls Potassium Chloride for Inj. Concentrate, USP, 40 mEq (2 mEq
Recalled 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
Hazard / Issue
Presence of Particulate; red and black particulate within the solution and embedded within the plastic vial identified as iron oxide
Issued by
FDA
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