Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Gambro Cartridge Blood Transport System for Hemodialysis Blood Set Recalled by Baxter Healthcare Corporation Due to complaints of kinked access lines observed during treatment...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Baxter Healthcare Corporation directly.
Affected Products
Gambro Cartridge Blood Transport System for Hemodialysis Blood Set, product code 106289 - Product Usage: intended for single use in a hemodialysis treatment using the Phoenix Dialysis Delivery Systems.
Quantity: 1460 devices
Why Was This Recalled?
complaints of kinked access lines observed during treatment using cartridge sets for hemodialysis treatments were received.
Where Was This Sold?
Worldwide distribution.
About Baxter Healthcare Corporation
Baxter Healthcare Corporation has 401 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report