PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: October 30, 2024 Initiated: September 19, 2024 #Z-0210-2025

Product Description

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

Reason for Recall

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

Details

Units Affected
6045 units
Distribution
Worldwide distribution.
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
Baxter Operating table TruSystem 7000 U (MB), Product codes: a) REF 1604786; b) REF 1604788; c) REF 1723633. Recalled by Baxter Healthcare Corporation. Units affected: 6045 units.
Why was this product recalled?
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 30, 2024. Severity: Moderate. Recall number: Z-0210-2025.