Baxter recalls Gambro Cartridge Blood Set Prime Line (product code 101025) for reported kinked access lines during hemodialysis treatments. This may cause treatment complications.
complaints of kinked access lines observed during treatment using cartridge sets for hemodialysis treatments were received.
Baxter is recalling Gambro Cartridge Blood Set Prime Line (product code 101025) used in hemodialysis treatments because users reported kinked access lines. This could lead to treatment complications if not addressed.
Kinked access lines during hemodialysis treatments can cause treatment complications. This happens when the cartridge sets become twisted or bent during use, potentially disrupting blood flow.
Hemodialysis patients using the Gambro Cartridge Blood Set Prime Line (product code 101025) are affected. Patients using this product for single-use hemodialysis treatments are most at risk.
Check for the product code 101025 on the Gambro Cartridge Blood Set Prime Line used in hemodialysis treatments. The product was sold with UDI 07332414007836 and all lots within expiry.
Look for product code 101025 on the Gambro Cartridge Blood Set Prime Line used in hemodialysis treatments.
The recall is due to reported kinked access lines during hemodialysis treatments, which could cause complications. Users should check if they have the recalled product.
The recall record does not specify a remedy, so users should check product details and contact their healthcare provider for guidance.
Check for product code 101025 on the Gambro Cartridge Blood Set Prime Line used in hemodialysis treatments. The product was sold with UDI 07332414007836 and all lots within expiry.
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1118-2021 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-1118-2021 from Baxter Healthcare. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
