FDA recall Z-0213-2025

Baxter Healthcare Corporation · Class II · device

Product

Baxter Operating Table TruSystem 7000 (dV), Product code REF 1841049

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-0213-2025