Baxter recalls Gambro Cartridge Blood Set (Product Code 101025) used in hemodialysis due to potential leak between venous connector and patient access. Affected units sold with specific lot numbers and UDI codes.
There is a potential leak between the venous patient connector and patient's hemodialysis access.
Baxter is recalling Gambro Cartridge Blood Sets used in hemodialysis treatments because they may leak between the venous connector and patient access. This leak could cause blood loss or infection risks during dialysis. Affected units have specific product codes and lot numbers.
The blood set may leak between the venous patient connector and the patient's hemodialysis access during use. This leak could lead to blood loss or infection if the leak occurs while the patient is being treated.
Hemodialysis patients using Gambro Cartridge Blood Sets with Product Code 101025 are most at risk. Patients using the product with specific lot numbers and UDI codes should check if their unit is affected.
Check for Product Code 101025 on the blood set. Affected units were sold with Lot 1000276191 and UDI code 37332414007837.
Look for Product Code 101025 on the blood set to confirm if it's affected.
Reach out to Baxter Healthcare Corporation for assistance with the recall if you have the affected product code.
The product may have a potential leak risk, so it's recommended to check if your unit is affected before use.
Check the Product Code and contact Baxter Healthcare Corporation for further instructions.
Look for Product Code 101025, Lot 1000276191, or UDI code 37332414007837 on the blood set.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-1684-2021 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-1684-2021 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.
