Baxter recalls MiniCap Extended Life PD Transfer Sets with Twist Clamp (part T5C4482) due to female connector separation in peritoneal dialysis use. Affected units have specific lot numbers and UDI/DI codes.
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 T5C:4482) used in peritoneal dialysis because the female connector may separate from the main body. This could lead to complications during dialysis treatments if the connection fails.
The female connector may separate from the main body of the transfer set during use in peritoneal dialysis. This separation could cause the dialysis solution to leak or the connection to fail, potentially leading to complications during treatment.
Peritoneal dialysis patients using the Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp (part number T5C4482) are affected. Patients using the specific lot numbers H23L06097 or H24A29033 are most at risk.
Check for the part number T5C4482 on the transfer set. Affected units have UDI/DI code 04987456422890 and lot/serial numbers H23L06097 or H24A29033.
Verify the part number T5C4482 and UDI/DI code 04987456422890 on the transfer set.
Baxter recalls this product due to complaints about the female connector separating from the main body during peritoneal dialysis use.
The affected part number is T5C4482 with UDI/DI code 04987456422890 and lot/serial numbers H23L06097 or H24A29033.
The recall record does not specify a remedy or fix for this issue.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0567-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0567-2025 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.
