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Baxter Healthcare Corporation recalls Gambro Cartridge Single Needle Conversion Kit, product code 101290 - Product Usage: intended for single use in a hemodia
Recalled February 24, 2021 · FDA recall Z-1119-2021 · Baxter Healthcare
Hazard
complaints of kinked access lines observed during treatment using cartridge sets for hemodialysis treatments were received. · FDA Class II
Units
385 devices
Sold at
Worldwide distribution.
Description
complaints of kinked access lines observed during treatment using cartridge sets for hemodialysis treatments were received.
Product
Gambro Cartridge Single Needle Conversion Kit, product code 101290 - 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 →