Baxter recalls Gambro hemodialysis blood sets with potential tubing disconnection risk. Affected units have specific lot numbers and product codes. Stop using immediately to prevent injury.
Potential disconnection of tubing set.
Baxter is recalling Gambro hemodialysis blood transport cartridges that may disconnect during use. This could cause blood loss or infection if not properly secured. Affected units have specific lot numbers and product codes.
The tubing set may disconnect during hemodialysis treatment, potentially causing blood loss or infection. This happens because the connection points are not securely fastened in normal use.
Hemodialysis patients using the Gambro Cartridge Low Volume Blood Transport System for single-use hemodialysis treatments. Patients using the affected lot numbers are most at risk.
Check for product code 114434 and lot numbers 1000201510, 1000206870, 1000214235, 1000218202, or 1000224530. The product is intended for single use in hemodialysis treatments.
Identify the product code (114434) and lot numbers listed in the recall notice.
Discontinue use of the affected blood transport system to prevent potential disconnection.
The product code is 114434.
Lot numbers 1000201510, 1000206870, 1000214235, 1000218202, and 1000224530 are affected.
Check for product code 114434 and the specific lot numbers listed in the recall notice.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-2195-2020 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-2195-2020 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.
