[Recalled] Baxter Operating Table TruSystem 7000 (dV) V, Product code REF 1841083 — The firm received customer reports stating that the batteries and their connect… | FDA 2024-09-19
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Baxter Operating Table TruSystem 7000 (dV) V, Product code REF 1841083 |
|---|---|
| Brand / manufacturer | Baxter Healthcare Corporation |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0216-2025 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 19 September 2024 |
| EAN / barcode | 00887761974227 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
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This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.