Baxter recalls Gambro Cartridge Blood Set Prime Line for potential tubing disconnection during hemodialysis treatments. Affected units have specific lot numbers and product codes.
Potential disconnection of tubing set.
Baxter is recalling Gambro Cartridge Blood Set Prime Line products used in hemodialysis treatments due to a risk of tubing disconnection. This could lead to treatment interruptions or complications if not addressed.
The tubing set can disconnect during use, potentially causing interruptions in hemodialysis treatments. This could lead to treatment complications or incomplete dialysis sessions if not properly secured.
Healthcare providers using hemodialysis equipment with the recalled Gambro Cartridge Blood Set Prime Line products are most at risk. Patients receiving dialysis treatments with these specific units may experience treatment interruptions.
Check for product code 101025 and lot numbers listed in the recall (e.g., 1000200708, 1000203117). The product is used in hemodialysis treatments with Dialysis Delivery Systems.
Verify your product code (101025) and lot numbers against the list provided in the recall notice.
The recall is due to potential disconnection of the tubing set during hemodialysis treatments, which could cause treatment interruptions or complications.
The recall notice does not specify a remedy, so check the product details against the listed lot numbers and contact Baxter Healthcare Corporation for further instructions.
The recall indicates a potential risk of tubing disconnection, so it is recommended to check product details and follow the manufacturer's guidance.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-2193-2020 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-2193-2020 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.
