AirLife™ FM2699Recalls & reported problems
Vyaire Medical, Inc. · AirLife™ Adult Cushion Nasal Cannula With Foam Ear Covers and 7 foot (2.1 m) Crush-Resistant Oxygen Tubing, and U/Connect-it™ Adapter · Class 2
All models of AirLife (25)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10190752117587), received between Jul 18, 2025 and Jul 18, 2025 — classified as 2 injuries.
The most frequently reported specific device problem is “Material Too Rigid or Stiff” (2 reports).
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
- Material Too Rigid or Stiff2
Patient problems
- Pressure Sore/Ulcer2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJul 18, 2025Material Too Rigid or Stiff; Material Too Rigid or Stiff
IT WAS REPORTED THAT THE PATIENT(S) ACQUIRED PRESSURE INJURY FROM THE NASAL CANNULAS. THERE WAS NO REPORT OF MEDICAL INTERVENTION. SINCE THERE WERE TWO REPORTS OF INJURY A SECONDARY MDR WILL BE SUBMITTED WITH THIS ONE TWO DOCUMENT BOTH INJURIES. THE SECOND MDR IS 1314417-2025-00049.
Patient problems: Pressure Sore/Ulcer
MAUDE report 22549427 ↗InjuryJul 18, 2025Material Too Rigid or Stiff; Material Too Rigid or Stiff
IT WAS REPORTED THAT THE PATIENT(S) ACQUIRED PRESSURE INJURY FROM THE NASAL CANNULAS. THERE WAS NO REPORT OF MEDICAL INTERVENTION. SINCE THERE WERE TWO REPORTS OF INJURY A SECONDARY MDR WILL BE SUBMITTED WITH THIS ONE TWO DOCUMENT BOTH INJURIES. THE FIRST MDR IS 1314417-2025-00048.
Patient problems: Pressure Sore/Ulcer
MAUDE report 22549422 ↗
Other Conserver, oxygen devices
- AirLife™ SFT2601Vyaire Medical, Inc. · Conserver, oxygen4 reports
- Evolution™ OM-900Inovo, Inc. · Conserver, Oxygen2 reports
- ACCUPULSE SINGLE LUMEN CONSERVING REGULATOR IN6505-L-BLUEInovo, Inc. · Conserver, Oxygen2 reports
- Drive OM-900AInovo, Inc. · Conserver, Oxygen2 reports
- SMARTDOSE CTOX-MN02Inovo, Inc. · Conserver, Oxygen1 report
- AirLife™ 002601Vyaire Medical, Inc. · Conserver, oxygen1 report
- AirLife™ SFT2692Vyaire Medical, Inc. · Conserver, oxygen1 report
- BONSAI OM-812Inovo, Inc. · Conserver, Oxygen1 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 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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