Z-0216-2025 Class II Ongoing
FDA device recall Z-0216-2025 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: N/A.
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
- N/A
Product Description
Baxter Operating Table TruSystem 7000 (dV) V, Product code REF 1841083
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 00887761974227, 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-0216-2025
- openFDA file date
- Oct 6, 2026
- Loaded by RegDataLab
- Oct 12, 2026