Baxter Healthcare Corporation: Medical Device Recall in 2024 - (Recall #: Z-0210-2025)

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 Operating table TruSystem 7000 U (MB), Product codes: a) REF 1604786; b) REF 1604788; c) REF 1723633

Product Classification:

Class II

Date Initiated: September 19, 2024

Date Posted: October 30, 2024

Recall Number: Z-0210-2025

Event ID: 95409

Reason for Recall:

The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.

Status: Ongoing

Product Quantity: 6045 units

Code Information:

a) REF 1604786, UDI/DI 00887761967533; b) REF 1604788, UDI/DI 00887761967526; c) REF 1723633, UDI/DI 00887761967519 ALL SERIAL NUMBERS

Distribution Pattern:

Worldwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated