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WatchCare P00697902Recalls & reported problems

Hill-Rom, Inc. · Hospital Bed Accessory, WatchCare System for VersaCare Bed Rev. K · 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. Sep 30, 2022Open, Classified

    Radio frequency emission from a functioning WatchCare device may potentially impact other devices (including, but not limited to telemetry devices, bladder scanner, fetal monitor/doppler, infusion pumps, and insulin pumps).

    Z-0144-2023 · Root cause: Device Design · FDA record ↗

Other ALARM, CONDITIONED RESPONSE ENURESIS devices

All ALARM, CONDITIONED RESPONSE ENURESIS devices →

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