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Baxter Healthcare Corporation recalls Empty IntraVia Container with Non-DEHP Fluid Path, 500mL Containers are intended for use in the preparation and admin
Recalled February 7, 2018 · FDA recall Z-0485-2018 · Baxter Healthcare
Hazard
A leak may allow for microbial contamination of the sterile fluid path. · FDA Class II
Units
29,088 units
Sold at
Distribution in the US and Canada.
Description
A leak may allow for microbial contamination of the sterile fluid path.
Product
Empty IntraVia Container with Non-DEHP Fluid Path, 500mL Containers are intended for use in the preparation and administration of drug admixtures.
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →