Z-0211-2025 Class II Ongoing
FDA device recall Z-0211-2025 was initiated by Baxter Healthcare Corporation on September 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: 397 units.
Recall Details
- Product Type
- Devices
- Report Date
- October 30, 2024
- Initiation Date
- September 19, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 397 units
Product Description
Baxter Operating Table TruSystem 7000, Product code REF 1841046
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
UDI/DI 00887761968714, All Serial Numbers