Baxter Operating Table TruSystem 7000 — Class II medical device recall Z-0213-2025
Ongoing recall by Baxter Healthcare Corporation, reported 2024-10-30. The firm received customer reports stating that the batteries and their connectors experienced electrical shor
| Recall number | Z-0213-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2024-09-19 |
| Classified | 2024-10-24 |
| Reported by FDA | 2024-10-30 |
| Quantity | 1,077 units |
| UPC / GTIN / UDI-DI | 00887761968691 |
| Model numbers | 1841049 |
Product
Baxter Operating Table TruSystem 7000 (dV), Product code REF 1841049
Reason for recall
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0213-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.