FDA Device recall Z-0210-2025
Baxter Operating table TruSystem 7000 U (MB), Product codes: a) REF 1604786
- FDA Device
- Class II
- ongoing
- Published 2024-10-30
On 2024-10-30 the FDA classified a Class II recall of Baxter Operating table TruSystem 7000 U (MB), Product codes: a) REF 1604786 by Baxter Healthcare, citing the firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0210-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-09-19 |
| Published | 2024-10-30 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Baxter Healthcare |
| Distribution | n/a |
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.
Identifiers
| code_info | a) REF 1604786, UDI/DI 00887761967533; b) REF 1604788, UDI/DI 00887761967526; c) REF 1723633, UDI/DI 00887761967519 ALL SERIAL NUMBERS |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0210-2025%22
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