MEDLINE MDT851BELTRecalls & reported problems
Medline Industries, Inc. · SELF-RELEASING ALARM BELT,MDT85 SERIES · Class 1
Data updated Oct 16, 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 10193489036633), received between Aug 11, 2026 and Aug 11, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Activation Problem” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Activation Problem1
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.
MalfunctionAug 11, 2026Activation Problem
It was reported that "6 belts that have been doing this" and "apparently they were doing it since taking them out of box."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50212890 ↗
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- POSEY 8309ELPosey Products, LLC · Monitor, Bed Patient2 deaths19 reports
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- 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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