Baxter recalls MiniCap Extended Life PD Transfer Sets with Twist Clamp (Part 5C4482) used in peritoneal dialysis due to potential PCB exposure risks. Affected units include all lots manufactured after H19I2:6088.
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 MiniCap Extended Life PD Transfer Sets with Twist Clamp (Part 5C4482) used in peritoneal dialysis because they may expose users to PCBs. This recall is due to potential exposure to non-dioxin-like PCBs during dialysis procedures.
The device may expose users to non-dioxin-like PCBs (polychlorinated biphenyls) during peritoneal dialysis. These chemicals are linked to health risks, though the specific risk level is not detailed in the recall.
People using peritoneal dialysis with this specific Baxter MiniCap set are affected. Those with peritoneal dialysis treatments are most at risk.
Check for the part number 5C4482 on the device. The product was sold with UDI/DI 00085412007731 and manufactured after H19I26088.
Look for part number 5C4482 and UDI/DI 00085412007731 on the device label.
The recall states potential exposure to PCBs, but does not specify if the product is unsafe to use. Baxter has issued a recall for potential risk, not immediate danger.
The recall does not provide specific action steps. You should check the device details and contact Baxter for further instructions.
The recall mentions potential exposure to non-dioxin-like PCBs, which are linked to health risks, but the specific risks are not detailed in the official notice.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0373-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0373-2025 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.
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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.
