DeVilbiss DV51UKRecalls & reported problems
Devilbiss Healthcare LLC · SLEEPCUBE STANDARD CPAP UK · Class 2
- 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 00885304002017), received between Feb 2, 2018 and Feb 2, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Arcing” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Arcing1
Patient problems
- No Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 2, 2018Arcing; Arcing
THE DEVILBISS HEALTHCARE'S (B)(4) DISTRIBUTOR REPORTED THE CPAP DV51UK,'S (J8) AC VOLTAGE POWER CONNECTOR SOLDERED TO THE INTERNAL PRINTED CIRCUIT BOARD (PCB) WAS ARCING. THE (B)(4) DISTRIBUTOR REPORTED THERE WAS NO PATIENT HARM.
Patient problems: No Information
MAUDE report 7237591 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.