Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, 100mL, VisIV Container, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-798
Recalled January 14, 2015 · FDA recall D-0334-2015 · Hospira
Hazard
Lack of Assurance of Sterility: The product has the potential for solution to leak at the administrative port. · FDA Class II
Units
30840 bags
Sold at
Nationwide
Description
Lack of Assurance of Sterility: The product has the potential for solution to leak at the administrative port.
Product
0.9% Sodium Chloride Injection, USP, 100mL, VisIV Container, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-7984-11
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →