# FDA recall Z-0329-2025

> **WISSNER-BOSSERHOFF GMBH** · Class II · device recall initiated 2022-07-11.

## Product

SafeControl handset (a component of the Sentida bed which moves and positions the bed), Model Numbers:  01-011539, 01-011541, 01-01198

## Reason for recall

When the handset is disconnected from the power mains, and mains operation is restored, the handset is reset to the preset Resident mode. In this mode, the backrest, legrest, and height adjustment can be moved.

## Distribution

US Nationwide distribution in the states of NC.

## Key facts

- **Recall number:** Z-0329-2025
- **Recalling firm:** WISSNER-BOSSERHOFF GMBH
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-07-11
- **Report date:** 2024-11-20

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Wickede (Ruhr), N/A, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0329-2025

## Citation

> AI Analytics. FDA recall Z-0329-2025. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-0329-2025. Source: US FDA. Licensed CC0.

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