WISSNER-BOSSERHOFF GMBH Hauptstr. 4-6 Wickede (Ruhr) Germany SafeControl handset (a component of the Sentida bed which moves and positions the bed), Model Numbers: 01-011539, 01-011541, 01-01198 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
SafeControl handset (a component of the Sentida bed which moves and positions the bed), Model Numbers: 01-011539, 01-011541, 01-01198
Brand
WISSNER-BOSSERHOFF GMBH Hauptstr. 4-6 Wickede (Ruhr) Germany
Lot Codes / Batch Numbers
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
Products Sold
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
WISSNER-BOSSERHOFF GMBH Hauptstr. 4-6 Wickede (Ruhr) Germany is recalling SafeControl handset (a component of the Sentida bed which moves and positions the bed), Model Number due to 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. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Wissner-bosserhoff issued an Urgent safety information notice along with supplement use instructions notice to its sole US consignee on 07/11/2022. The notice explained the problem, risk to patient, and requested the user update the IFU for the device. Distributors were directed to notify their customers.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026