Recall Z-0210-2025— Baxter Healthcare Corporation
Class II · Ongoing
Class II FDA medical device recall by Baxter Healthcare Corporation, initiated 2024-09-19. FDA's recall record names no specific 510(k) clearance for this event. Product: Baxter Operating table TruSystem 7000 U (MB), Product codes: a) REF 1604786; b) REF 1604788; c) REF 1723633. Reason: The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke..
- Recalling firm
- Baxter Healthcare Corporation
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-09-19
- Firm location
- Deerfield, IL, United States
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.