Hospira Inc. recalls Sterile Water for Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 NDC
Recalled December 3, 2014 · FDA recall D-0287-2015 · 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
153,504 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
Sterile Water for Injection, USP, 1000 mL container, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045 NDC 0409-7990-09.
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →