Baxter Healthcare Corporation: Medical Device Recall in 2024 - (Recall #: Z-0562-2025)

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 with Twist Clamp, Part Number 5C4483; use in Peritoneal Dialysis

Product Classification:

Class II

Date Initiated: October 23, 2024

Date Posted: December 4, 2024

Recall Number: Z-0562-2025

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: 62,718

Code Information:

UDI/DI 00085412007748, Lot/Serial Numbers: H23J10051, H23J23062, H23K20066, H24C08033, H24E16080, H24F12046, H24F17045, H24G02045, H24I02090

Distribution Pattern:

Worldwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated