Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, 250 mL single dose Flex
Recalled Product
0.9% Sodium Chloride Injection, USP, 250 mL single dose Flexible Plastic Container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-7983-02
Hazard / Issue
Lack of Assurance of Sterility: The product has the potential for solution to leak at or near the administrative port of the primary container.
Issued by
FDA
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