WatchCareRecalls & reported problems across all models
Hill-Rom, Inc. · 4 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
4 open recalls name at least one WatchCare model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 4
We found 4 models of WatchCare by Hill-Rom, Inc. in the FDA's device registry (GUDID). None of them is named in an adverse event report in our data.
4 FDA recall records name at least one of these models by its device identifier, 4 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
WatchCare recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- 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-0145-2023 · Root cause: Device Design · Recall details · FDA record ↗
- 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 · Recall details · FDA record ↗
- 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-0143-2023 · Root cause: Device Design · Recall details · FDA record ↗
- 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-0142-2023 · Root cause: Device Design · Recall details · FDA record ↗
WatchCare models
4 models, most reported first. Each model has its own page with its reports, recalls and device details.
- WatchCare P00697905ALARM, CONDITIONED RESPONSE ENURESIS1 recall0 reports
- WatchCare P00697901ALARM, CONDITIONED RESPONSE ENURESIS1 recall0 reports
- WatchCare P00697902ALARM, CONDITIONED RESPONSE ENURESIS1 recall0 reports
- WatchCare P00697903ALARM, CONDITIONED RESPONSE ENURESIS1 recall0 reports
Other Hill-Rom, Inc. products
- Centrella Bed2 models · 2,021 reports · 2 recalls
- VersaCare Med Surg Bed2 models · 1,200 reports
- pro+18 models · 36 reports · 13 recalls
- Voalte Nurse Call2 models · 419 reports · 2 recalls
- ALLEN24 models · 73 reports · 5 recalls
- NaviCare Nurse Call Systems3 models · 99 reports · 2 recalls
- CompellaSurface3 models · 87 reports · 1 recall
- Progressa Surface13 models · 8 reports · 1 recall
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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