Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, a) 50 mL (NDC 0409-7984
Recalled Product
0.9% Sodium Chloride Injection, USP, a) 50 mL (NDC 0409-7984-13), b) 50 mL (NDC 0409-7984-36), c) 100 mL (0409-7984-37), Rx Only, Hospira, Inc., Lake Forest, IL 60045
Hazard / Issue
Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot #: a) 11-085-JT, Exp 11/13; b) 06-111-JT, Exp 12/12, c) 93-030-JT, 14-044-JT, Exp 9/12
View official government recall
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