Baxter recalls MiniCap Extended Life PD Transfer Sets with titanium spike for peritoneal dialysis due to female connector separation complaints. Affected units have specific part numbers and serials.
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 titanium spikes for peritoneal dialysis because users have reported the female connector separating from the main body. This could lead to improper dialysis treatment if the connection fails during use.
The female connector can separate from the main body of the transfer set during use, which may cause improper dialysis treatment. This separation could lead to complications if the connection fails while the patient is being treated.
Peritoneal dialysis patients using the Baxter MiniCap Extended Life PD Transfer Set with titanium spike (part number T5C4326K) are most at risk. Patients who have the specific serial numbers listed in the recall are affected.
Check for the part number T5C4326K on the transfer set. Affected units have specific serial numbers: H23J02025, H23L04043, H23L05057, H23L05073, H24A29041, H24C01061, H24E13061, H24G15062.
Inspect the female connector for separation from the main body of the transfer set.
Baxter has received complaints about the female connector separating from the main body of the transfer set, which could lead to improper dialysis treatment.
The affected part number is T5C4326K. Affected units have specific serial numbers: H23J02025, H23L04043, H23L05057, H23L05073, H24A29041, H24C01061, H24E13061, H24G15062.
The recall does not require immediate stop use; however, you should check for connector separation before continuing use.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0569-2025 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0569-2025 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.
