Z-0210-2025 Class II Ongoing
FDA device recall Z-0210-2025 was initiated by Baxter Healthcare Corporation on Sep 19, 2024 and is designated Class II. Reason for recall: The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke. The recall status is ongoing. Affected quantity: 6045 units.
Recall Details
- Product Type
- Devices
- Report Date
- Oct 30, 2024
- Initiation Date
- Sep 19, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 6045 units
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.
Distribution Pattern
Worldwide distribution.
Code Information
a) REF 1604786, UDI/DI 00887761967533; b) REF 1604788, UDI/DI 00887761967526; c) REF 1723633, UDI/DI 00887761967519 ALL SERIAL NUMBERS
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0210-2025
- openFDA file date
- Oct 6, 2026
- Loaded by RegDataLab
- Oct 12, 2026