Hospira Inc. recalls Sodium Acetate Injection, USP, 40 mEq/20 ml (2 mEq/mL) 20 mL
Recalled Product
Sodium Acetate Injection, USP, 40 mEq/20 ml (2 mEq/mL) 20 mL Single-Dose Fliptop, Rx only, HOSPIRA, INC. LAKE FOREST, IL 60045 USA, NDC 0409-7299-73
Hazard / Issue
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot 23-320-DK and 23-321-DK Exp. 11/14
View official government recall
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