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Baxter Healthcare Corporation recalls Gambro Cartridge Blood Set, Product Code 101025 - Product Usage: intended for single use in a hemodialysis treatment usi
Recalled June 2, 2021 · FDA recall Z-1684-2021 · Baxter Healthcare
Hazard
There is a potential leak between the venous patient connector and patient's hemodialysis access. · FDA Class II
Units
17,487 units
Sold at
Worldwide distribution - United States distribution and the countries of Canada, Korea, and Norway.
Description
There is a potential leak between the venous patient connector and patient's hemodialysis access.
Product
Gambro Cartridge Blood Set, Product Code 101025 - Product Usage: intended for single use in a hemodialysis treatment using the Phoenix Dialysis Delivery Systems.
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →