Baxter Healthcare Corporation: Medical Device Recall in 2024 - (Recall #: Z-0378-2025)

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 R5C4482E; use in Peritoneal Dialysis

Product Classification:

Class I

Date Initiated: October 21, 2024

Date Posted: November 27, 2024

Recall Number: Z-0378-2025

Event ID: 95525

Reason for Recall:

Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using certain peritoneal dialysis and hemodialysis devices.

Status: Ongoing

Product Quantity: 58,680 units

Code Information:

UDI/DI 05413760375861, Lot/Serial Numbers: All lots including and manufactured after H19K04041

Distribution Pattern:

Worldwide Distribution (US Nationwide distribution)

Voluntary or Mandated:

Voluntary: Firm initiated