Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, 250 mL, Rx Only, Hospira Inc., Lake Forest, IL, 60045, USA, NDC 0409-7983-02
Recalled April 29, 2015 · FDA recall D-0969-2015 · Hospira
Hazard
Presence of Particulate Matter; Hospira has identified the particulate as a human hair, sealed in the bag at the additive port area. · FDA Class I
Units
661,128 containers
Sold at
Nationwide
Description
Presence of Particulate Matter; Hospira has identified the particulate as a human hair, sealed in the bag at the additive port area.
Product
0.9% Sodium Chloride Injection, USP, 250 mL, 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 →