Baxter recalls MiniCap Extended Life PD Transfer Sets with Twist Clamp (R5C4484) due to female connector separation in peritoneal dialysis. Affected units have specific lot numbers and part numbers.
There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
Baxter is recalling MiniCap Extended Life PD Transfer Sets with Twist Clamp (part number R5C:4484) used in peritoneal dialysis because the female connector may separate from the main body. This could lead to complications during dialysis treatments.
The female connector may separate from the main body of the transfer set during use. This separation could cause leaks or other complications in peritoneal dialysis treatments, potentially leading to health issues if not addressed.
Peritoneal dialysis patients using the Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp (part number R5C4484) are affected. Patients with specific lot numbers (H23J23039) are most at risk.
Check for the part number R5C4484 on the transfer set. Affected units have lot/serial number H23J23039 and UDI/DI 00085412050768.
Look for part number R5C4484 and lot/serial number H23J23039 on the transfer set.
Baxter recalls these transfer sets due to complaints about the female connector separating from the main body, which could cause complications during peritoneal dialysis.
Check the part number and lot/serial number on your transfer set. If it matches R5C4484 and H23J23039, contact Baxter for guidance.
The recall record does not specify a remedy; affected users should contact Baxter for further instructions.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0566-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0566-2025 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.
