Hospira Inc. recalls 5% Dextrose and 0.9% Sodium Chloride Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Fo
Recalled December 3, 2014 · FDA recall D-0282-2015 · Hospira
Hazard
Lack of Assurance of Sterility: Potential of punctures through the overwrap and primary container which may result in IV bag leaks. · FDA Class II
Units
340,272 bags
Sold at
Nationwide, Puerto Rico, and U.S. Virgin Islands.
Description
Lack of Assurance of Sterility: Potential of punctures through the overwrap and primary container which may result in IV bag leaks.
Product
5% Dextrose and 0.9% Sodium Chloride Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7941-09.
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →