Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7
Recalled May 13, 2015 · FDA recall D-0976-2015 · Hospira
Hazard
Presence of Particulate Matter: Confirmed finding of human hair floating in IV solution. · FDA Class I
Units
9,912 VisIV flex containers
Sold at
Nationwide.
Description
Presence of Particulate Matter: Confirmed finding of human hair floating in IV solution.
Product
0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-25.
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →