AirLife™ 002601Recalls & reported problems
Vyaire Medical, Inc. · AirLife™ Infant Cushion Nasal Cannula 7 feet (2.1 m) Crush-Resistant Oxygen Tubing · Class 2
Data updated Oct 13, 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 10190752115071), received between Dec 2, 2020 and Dec 2, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Improper Flow or Infusion” (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
- Improper Flow or Infusion1
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.
MalfunctionDec 2, 2020Improper Flow or Infusion; Improper Flow or Infusion
THE CUSTOMER REPORTED THAT THE CANNULA CUSHION INFANT W/7FT TB 50/CS EXPERIENCED LACK OF FLOW. THE CUSTOMER CONFIRMED THAT THERE WAS NO PATIENT HARM ASSOCIATED WITH THE REPORTED EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10932129 ↗
Other Conserver, oxygen devices
- AirLife™ SFT2601Vyaire Medical, Inc. · Conserver, oxygen4 reports
- AirLife™ FM2699Vyaire Medical, Inc. · Conserver, oxygen2 reports
- Evolution™ OM-900Inovo, Inc. · Conserver, Oxygen2 reports
- Drive OM-900AInovo, Inc. · Conserver, Oxygen2 reports
- ACCUPULSE SINGLE LUMEN CONSERVING REGULATOR IN6505-L-BLUEInovo, Inc. · Conserver, Oxygen2 reports
- EVOLUTION OM-900AInovo, Inc. · Conserver, Oxygen1 report
- Drive P-224Drive Devilbiss Healthcare · Conserver, oxygen1 report
- AirLife™ SFT2699Vyaire Medical, 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 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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