Class II — WISSNER-BOSSERHOFF GMBH
| Recalling firm | wissner-bosserhoff GmbH |
|---|---|
| Registered facility | WISSNER-BOSSERHOFF GMBH (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| 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. |
| Product | SafeControl handset (a component of the Sentida bed which moves and positions the bed), Model Numbers: 01-011539, 01-011541, 01-01198 |
| Quantity | 77 units |
| Distribution | US Nationwide distribution in the states of NC. |
| Initiated | 2022-07-11 |
| Classified | 2024-11-08 |
| Recall number | Z-0329-2025 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — WISSNER-BOSSERHOFF GMBH (Z-0329-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/95490/
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