WISSNER-BOSSERHOFF GMBH: Medical Device Recall in 2024 - (Recall #: Z-0329-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: July 11, 2022

Date Posted: November 20, 2024

Recall Number: Z-0329-2025

Event ID: 95490

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.

Status: Ongoing

Product Quantity: 77 units

Code Information:

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

Distribution Pattern:

US Nationwide distribution in the states of NC.

Voluntary or Mandated:

Voluntary: Firm initiated