Baxter recalls Gambro Cartridge Low Volume Blood Transport System for hemodialysis treatments due to reported kinked access lines during use. This may affect blood flow safety in dialysis treatments.
complaints of kinked access lines observed during treatment using cartridge sets for hemodialysis treatments were received.
Baxter is recalling Gambro Cartridge Low Volume Blood Transport Systems used in hemodialysis treatments because users reported kinked access lines during treatments. This could potentially cause blood flow issues if the lines become kinked.
Kinked access lines during hemodialysis treatments can cause blood flow issues. This may lead to complications if the lines become kinked while the patient is being treated.
Hemodialysis patients using the Gambro Cartridge Low Volume Blood Transport System with product code 114434 are affected. Patients using this system for dialysis treatments are most at risk.
Check for the product code 114434 on the Gambro Cartridge Low Volume Blood Transport System used with Phoenix Dialysis Delivery Systems. This system is intended for single use in hemodialysis treatments.
Look for product code 114434 on the Gambro Cartridge Low Volume Blood Transport System.
The recall is due to reported kinked access lines during hemodialysis treatments, but the product is generally safe if used correctly.
Check for product code 114434 on the Gambro Cartridge Low Volume Blood Transport System used with Phoenix Dialysis Delivery Systems.
The recall does not specify a remedy, so contact your healthcare provider for guidance on next steps.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1122-2021 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1122-2021 from Baxter. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
