Baxter Healthcare Corporation: Medical Device Recall in 2024 - (Recall #: Z-0569-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Baxter MiniCap Extended Life PD Transfer Set (short) with Titanium Spike, Part Number T5C4326K; use in Peritoneal Dialysis

Product Classification:

Class II

Date Initiated: October 23, 2024

Date Posted: December 4, 2024

Recall Number: Z-0569-2025

Event ID: 95524

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 13376 units

Code Information:

UDI/DI 0085412150703, Lot/Serial Numbers: H23J02025, H23L04043, H23L05057, H23L05073, H24A29041, H24C01061, H24E13061, H24G15062

Distribution Pattern:

Worldwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated