# FDA recall Z-0210-2025

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2024-09-19.

## Product

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

Worldwide distribution.

## Key facts

- **Recall number:** Z-0210-2025
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-09-19
- **Report date:** 2024-10-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0210-2025

## Citation

> AI Analytics. FDA recall Z-0210-2025. Retrieved 2026-09-14 from https://api.ai-analytics.org/recall/Z-0210-2025. Source: US FDA. Licensed CC0.

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