Baxter recalls MiniCap Extended Life PD Transfer Sets with Twist Clamp EX Short (Part T5C4484) used in peritoneal dialysis due to potential PCB exposure. Affected units include all lots manufactured after H20B11074.
Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using certain peritoneal dialysis and hemodialysis devices.
Baxter is recalling a specific peritoneal dialysis transfer set because it may expose users to PCBs (a type of chemical) during use. This recall affects people who use the device for peritoneal dialysis, and the risk involves potential health effects from chemical exposure.
The device may release non-dioxin-like PCBs (chemicals) during peritoneal dialysis. These chemicals can potentially cause health effects if they enter the body through the dialysis process.
People using Baxter's MiniCap Extended Life PD Transfer Set with Twist Clamp EX Short for peritone:al dialysis are affected. Those with peritoneal dialysis who use this specific product are most at risk.
Check for the product name 'Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp EX Short' and part number T5C4484. The device was sold with lot/serial numbers starting with all lots including those manufactured after H20B11074.
Identify the part number T5C4484 and lot/serial numbers starting with all lots including those manufactured after H20B11074.
The recall states there is a potential risk of exposure to PCBs, but the product is not considered unsafe for normal use. Baxter has issued a recall to address this concern.
The recall does not specify a remedy, so you should check with Baxter directly for guidance on next steps.
Look for the part number T5C4484 and lot/serial numbers starting with all lots including those manufactured after H20B11074.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0382-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0382-2025 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.
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.
