Class II

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

Baxter Healthcare Corporation · September 19, 2024

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.

Quantity Affected

6045 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0210-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.