Baxter Healthcare Corporation: Medical Device Recall in 2024 - (Recall #: Z-0327-2025)

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 AK 98 Dialysis Machine, Hemodialysis Delivery System, Product Code 955607

Product Classification:

Class I

Date Initiated: October 16, 2024

Date Posted: November 20, 2024

Recall Number: Z-0327-2025

Event ID: 95527

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: 1100 units

Code Information:

UDI/DI 07332414124519, All serials with runtime less than 500 hours

Distribution Pattern:

US Nationwide distribution and worldwide

Voluntary or Mandated:

Voluntary: Firm initiated