Nox RIP Belts Disposable Large NOX-RIPDL20Recalls & reported problems
Nox Medical ehf. · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 15694311110187), received between Jul 15, 2020 and Jul 15, 2020 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Rash1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 15, 2020Adverse Event Without Identified Device or Use Problem
THE PATIENT DESCRIBED THAT THEY DEVELOPED CONTACT DERMATITIS ON THE ARMS AFTER UNDERGOING A HOME SLEEP STUDY WITH THE DEVICE WHICH REQUIRED ADMINISTRATION OF ORAL STEROIDS TO TREAT THE RASH.
Patient problems: Rash
MAUDE report 10275118 ↗
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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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