Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection, USP, 100 mL VIAFLEX Container, Rx Only, Baxter Healthcare Corporation, Deerfield IL 600
Recalled July 19, 2017 · FDA recall D-0973-2017 · Baxter Healthcare
Hazard
Lack of Assurance of Sterility: Bags have the potential to leak. · FDA Class II
Units
295,200 bags
Sold at
Nationwide, Puerto Rico and Saudi Arabia
Description
Lack of Assurance of Sterility: Bags have the potential to leak.
Product
0.9% Sodium Chloride Injection, USP, 100 mL VIAFLEX Container, Rx Only, Baxter Healthcare Corporation, Deerfield IL 60015 USA, Product Code: 2B1309, NDC: 0338-0049-38
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →