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sentida 1 19-0990Recalls & reported problems

WISSNER-BOSSERHOFF GmbH · Basic electric home bed · Class 2

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Jul 11, 2022Open, Classified

    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.

    Z-0329-2025 · Root cause: Device Design · FDA record ↗

Other Bed, Therapeutic, Ac-Powered, Adjustable Home-Use devices

All Bed, Therapeutic, Ac-Powered, Adjustable Home-Use devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.