Cavagna VIPROXY 1 TouchRecalls & reported problems
Cavagna North America Inc · Gas Cylinder Pressure Regulator. Analog pressure indicator · Class 1
Data updated Oct 13, 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 00850009834102), received between Apr 27, 2026 and Apr 27, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “No Audible Alarm” (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.
Reports received per month
Most reported problems
Device problems
- No Audible Alarm1
Patient problems
- Hypoxia1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 27, 2026No Audible Alarm
(E)(1) REPORTED THAT A PATIENT RECEIVING SUPPLEMENTAL OXYGEN FROM A PORTABLE OXYGEN CYLINDER EQUIPPED WITH A GRAB N' GO REGULATOR. THE REGULATOR WAS REPORTEDLY SET TO DELIVER OXYGEN AT 4 L/MIN. DURING USE, THE CYLINDER INDICATED IT WAS IN FILL MODE, AND THE PRESSURE INDICATOR DISPLAYED APPROXIMATELY 43 PSI. NO AUDIBLE ALARM WAS TRIGGERED. THE PATIENT WAS OBSERVED TO HAVE DECREASED OXYGEN SATURATION TO 83% AND WAS REPORTED TO BE HYPOXIC. IN RESPONSE, OXYGEN THERAPY WAS INCREASED TO 6 L/MIN VIA NASAL CANNULA, RESULTING IN THE PATIENT VITALS RETURNING TO PRE-EVENT LEVELS.
Patient problems: Hypoxia
MAUDE report 24998284 ↗
Other Regulator, Pressure, Gas Cylinder devices
- ISPAN 8065797303Alcon Laboratories, Inc. · REGULATOR, PRESSURE, GAS CYLINDER56 reports
- Medline HCS8708MMedline Industries, Inc. · REGULATOR, PRESSURE, GAS CYLINDER10 reports
- Medline HCS8715MAMedline Industries, Inc. · REGULATOR, PRESSURE, GAS CYLINDER9 reports
- Mini CGA 870 style regulator; 0-15 lpm RES043Sunset Healthcare Solutions, Inc. · Regulator, Pressure, Gas Cylinder2 reports
- EM L280-220KAllied Medical, LLC · Regulator, Pressure, Gas Cylinder2 reports
- Drive 18302GDELDrive Devilbiss Healthcare · REGULATOR, PRESSURE, GAS CYLINDER1 death1 report
- MediTec 0721109USGCE, s.r.o. · Regulator, Pressure, Gas Cylinder1 report
- Western/Scott Fetzer M1-540-15FMWestern Enterprises · Regulator, Pressure, Gas Cylinder1 report
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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