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WatchCare P00697903Recalls & reported problems

Hill-Rom, Inc. · Hospital Bed Accessory, Watch Care System for Progressa Bed · Class 2

All models of WatchCare (4)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

  1. Sep 30, 2022Class IOpen, 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-0143-2023 · Root cause: Device Design · Recall details · FDA record ↗

Other ALARM, CONDITIONED RESPONSE ENURESIS devices

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Sources and updates

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