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FDAFDA · Food and drugs·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

Published November 20, 2024 · Recall initiated: July 11, 2022

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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.

What to do

Voluntary: Firm initiated · E-Mail

Recall details

Manufacturer
WISSNER-BOSSERHOFF GMBH
Distributor
US Nationwide distribution in the states of NC.
Lot
UDI/DI 4050621100401, 19-0990 UDI/DI 4050621100012, 19-1062 UDI/DI 4050621100432, 19-1152 UDI/DI 4050621100449, 19-1119 UDI/DI 4050621100470, 19-1155 UDI/DI 4050621100487, 19-1156
Risk classification
Class II
Area (FDA)
device
Country
Germany

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