Hospira Inc. recalls Heparin Sodium 2000 USP Heparin Units per 1000 mL (2 USP Heparin Units/mL) in 0.9% Sodium Chloride Injection, Rx only. H
Recalled February 5, 2014 · FDA recall D-1036-2014 · Hospira
Hazard
Lack of Assurance of Sterility; potential leakage from administrative port. · FDA Class II
Units
27780 bags
Sold at
Nationwide including Puerto Rico
Description
Lack of Assurance of Sterility; potential leakage from administrative port.
Product
Heparin Sodium 2000 USP Heparin Units per 1000 mL (2 USP Heparin Units/mL) in 0.9% Sodium Chloride Injection, Rx only. Hospira, Lake Forest, IL 60045. NDC 0409-7620-59.
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →