FDA recall Z-0216-2025

Baxter Healthcare Corporation · Class II · device

Product

Baxter Operating Table TruSystem 7000 (dV) V, Product code REF 1841083

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-0216-2025