Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, 250 mL single dose Flexible Plastic Container, Rx only, Hospira, Inc., Lake Forest,
Recalled June 26, 2013 · FDA recall D-608-2013 · Hospira
Hazard
Lack of Assurance of Sterility: The product has the potential for solution to leak at or near the administrative port of the primary container. · FDA Class II
Units
676,872 containers
Sold at
Nationwide and Puerto Rico
Description
Lack of Assurance of Sterility: The product has the potential for solution to leak at or near the administrative port of the primary container.
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
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →