M200-C Fall Monitor (M200 With Closed Battery Compartment Cover)Recalls & reported problems
Securitas Healthcare LLC · M200-C Fall Monitor (M200 With Closed Battery Compartment Cover) · 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 00840948101595), received between Mar 24, 2022 and Mar 24, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Overheating of Device” (1 report).
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.
Most reported problems
Device problems
- Overheating of Device1
- Premature Discharge of Battery1
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.
MalfunctionMar 24, 2022Premature Discharge of Battery; Overheating of Device
IT WAS REPORTED OF NEARLY 30 INSTANCES OF BED ALARM'S BATTERIES WERE NOT ABLE TO HOLD A CHARGE AND WERE OVERHEATING WHILE IN USE WITH PATIENTS. THE SPAN OF THESE INCIDENTS INCLUDED SEVERAL LOT NUMBERS AND IN SEVERAL DIFFERENT LOCATIONS. NO EVIDENCE OF HARM TO ANY PATIENT WAS NOTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13886131 ↗
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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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