Baxter recalls MiniCap Extended Life PD Transfer Sets with Part Number 5C4482S 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 Part Number 5C4482S used in peritoneal dialysis. The recall is due to complaints about the female connector separating from the main body, which could lead to complications during dialysis treatments.
The female connector may separate from the main body during use, potentially causing leaks or disruptions in the dialysis process. This separation could lead to complications if the system is not properly reconnected.
Patients using peritoneal dialysis with the specific Baxter MiniCap Extended Life PD Transfer Set model are affected. Those with the listed lot/serial numbers are most at risk.
Check for the part number 5C4482S on the transfer set. The lot/serial numbers listed (H23J13063, H23J26081, etc.) indicate affected units sold for peritoneal dialysis.
Inspect the female connector for signs of separation from the main body before use.
Reach out to Baxter Healthcare Corporation for assistance with the recall process.
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 5C4482S for the MiniCap Extended Life PD Transfer Set.
Check the lot/serial numbers listed: H23J13063, H23J26081, H24B18059, H24B19065, H24B19099, H24B20071, H24C18065, H24E22062, H24F11048.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0561-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0561-2025 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.
