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AirLife™ SFT2692Recalls & reported problems

Vyaire Medical, Inc. · AirLife™ Pediatric Cushion Nasal Cannula With 7 foot (2.1 m) Crush-Resistant Oxygen Tubing, and U/Connect-It Adapter · Class 2

All models of AirLife (25)

Data updated Oct 18, 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 10190752117808), received between Sep 19, 2022 and Sep 19, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Inadequacy of Device Shape and/or Size” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Inadequacy of Device Shape and/or Size1
  • No Flow1

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.

  • MalfunctionSep 19, 2022Inadequacy of Device Shape and/or Size; No Flow; Inadequacy of Device Shape and/or Size; No Flow

    IT WAS REPORTED TO VYAIRE MEDICAL THAT THE CANNULA SOFT PED W/U-CON 7FT TB 50/CS DOES NOT REACH UP THE CUSTOMER'S NOSE, AND THE OPENING IS NARROW AND TOO SHORT. THE CUSTOMER WAS NOT ABLE TO GET ANY OXYGEN THROUGH THE CANNULA. AT THIS TIME, THE CUSTOMER HAS NOT PROVIDED ANY INFORMATION REGARDING PATIENT HARM OR INJURY ASSOCIATED WITH THE REPORTED EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15452336 ↗

Other Conserver, oxygen devices

All Conserver, oxygen devices →

Sources and updates

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