Wickede (Ruhr), N/A, Germany
WISSNER-BOSSERHOFF GMBH recalls
1 recall recorded since 2018, most recently on 11 July 2022. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 11 July 2022
- Reason
- 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.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0329-2025
- SafeControl handset (a component of the Sentida bed which moves and positions the bed), Model Numbers: 01-011539, 01-011541, 01-01198
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.