Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall 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

U.S. FDA — Device Enforcement · Germany · 2022-07-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0329-2025
Date of alert
2022-07-11
Country / jurisdiction
Germany
Risk level
Class II
Risk type
recall
Brand
WISSNER-BOSSERHOFF GMBH
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
4050621100401
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.