Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection USP, 250 mL VIAFLEX Container bag, Rx only, Baxter Healthcare Corporation, Deerfield, IL
Recalled July 19, 2017 · FDA recall D-0957-2017 · Baxter Healthcare
Hazard
Lack of Assurance of Sterility: Customer complaints for leaking bags. · FDA Class II
Units
131,904 bags
Sold at
Nationwide in USA
Description
Lack of Assurance of Sterility: Customer complaints for leaking bags.
Product
0.9% Sodium Chloride Injection USP, 250 mL VIAFLEX Container bag, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015; Distributed in Canada by Baxter Corporation, Toronto, Ontario, Canada, Product Code: 2B1322, NDC 0338-0049-02.
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →