Baxter recalls MiniCap Extended Life PD Transfer Sets with Twist Clamp (part 5C448: 5C4482EJ) for potential female connector separation during peritoneal dialysis use.
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 5C4482EJ) used in peritoneal dialysis because complaints indicate 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 disruptions in the peritoneal dialysis process, potentially leading to complications.
Peritoneal dialysis patients using the Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp (part number 5C4482EJ) are affected. Patients with the specific lot/serial numbers listed are at highest risk.
Check for the part number 5C4482EJ on the transfer set. Look for lot/serial numbers H24C19063, H24G22092, or H24G25061 on the packaging or label.
Inspect the female connector for signs of separation from the main body of the transfer set.
Reach out to Baxter Healthcare Corporation for guidance on next steps if separation is observed.
Baxter is recalling these transfer sets due to complaints about the female connector separating from the main body during peritoneal dialysis use.
The affected part number is 5C4482EJ, with lot/serial numbers H24C19063, H24G22092, and H24G25061.
The recall record does not specify a fix; users should check for separation and contact Baxter for guidance.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0560-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0560-2025 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.
