Hospira Inc. recalls 0.9% Sodium Chloride Injection USP, 100 mL Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7984-23,
Recalled March 13, 2013 · FDA recall D-183-2013 · Hospira
Hazard
Lack of Assurance of Sterility: There is the potential for solution to leak from the administrative port to the fill tube seal. · FDA Class II
Units
325,056 bags
Sold at
Nationwide
Description
Lack of Assurance of Sterility: There is the potential for solution to leak from the administrative port to the fill tube seal.
Product
0.9% Sodium Chloride Injection USP, 100 mL 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 →