Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. Lake Forest, IL 60045 --- NDC 040
Recalled September 4, 2013 · FDA recall D-922-2013 · Hospira
Hazard
Presence of Particulate Matter; product may contain fibrous material · FDA Class I
Units
264,432 bags
Sold at
Nationwide
Description
Presence of Particulate Matter; product may contain fibrous material
Product
0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. Lake Forest, IL 60045 --- NDC 0409-7984-23
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →