Stanley Healthcare RM-73030Recalls & reported problems
Renu Medical, Inc · Bed-Check ST Chair Sensormat · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00816317024024), received between Dec 10, 2024 and Dec 10, 2024 — classified as 1 malfunction.
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.
Reports received per month
Most reported problems
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 10, 2024
SENSORMAT WAS IN PLACE UNDER PATIENT AND ELECTRICAL INTERFERENCE NOTED ON TELEMETRY MONITOR. MANUFACTURER RESPONSE FOR MONITOR, BED PATIENT, STANLEY HEALTHCARE (PER SITE REPORTER). UNKNOWN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20891706 ↗
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- Voalte Patient Safety 4.0Hill-Rom, Inc. · MONITOR, BED PATIENT1 recall0 reports
- NaviCare® Patient Safety Systems 3.9Hill-Rom, Inc. · MONITOR, BED PATIENT1 recall0 reports
- Cubby Beds KIT10001Sensory Medical, Inc. · Monitor, Bed Patient30 reports
- Medline MDT8450YMedline Industries, Inc. · MONITOR, BED PATIENT29 reports
- POSEY 8309ELPosey Products, LLC · Monitor, Bed Patient2 deaths19 reports
- POSEY 8399Posey Products, LLC · Monitor, Bed Patient19 reports
- POSEY 8645WLPosey Products, LLC · Monitor, Bed Patient17 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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