FDA recall Z-0210-2025

Product

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.

Distribution

Worldwide distribution.

Key facts

Status

Ongoing

Initiation date

2024-09-19

Report date

2024-10-30

Voluntary/Mandated

Voluntary: Firm initiated

Location

Deerfield, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0210-2025