Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection, USP, 100 mL MINI-BAG VIAFLEX Container, Single Dose Container, Rx Only, Baxter Healthcar
Recalled September 30, 2015 · FDA recall D-1816-2015 · Baxter Healthcare
Hazard
Lack of Assurance of Sterility: Recalling firm reported a complaint for mold on the interior surface of the overpouch. · FDA Class II
Units
139,104 Bags
Sold at
Nationwide and Puerto Rico
Description
Lack of Assurance of Sterility: Recalling firm reported a complaint for mold on the interior surface of the overpouch.
Product
0.9% Sodium Chloride Injection, USP, 100 mL MINI-BAG VIAFLEX Container, Single Dose Container, Rx Only, Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-0049-38
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →