Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409
Recalled August 14, 2013 · FDA recall D-836-2013 · Hospira
Hazard
Presence of Particulate Matter: reports of small grey/brown particles found in the primary container identified as brass particulates · FDA Class I
Units
691,356 containers
Sold at
Nationwide
Description
Presence of Particulate Matter: reports of small grey/brown particles found in the primary container identified as brass particulates
Product
0.9% Sodium Chloride Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09.
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →