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AirLife 2D0735XRecalls & reported problems

Airlife · Sterile Water for Inhalation · 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 10190752196445), received between Jul 17, 2023 and Jul 17, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Gas/Air Leak” (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

  • Gas/Air Leak1
  • Leak/Splash1

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.

  • MalfunctionJul 17, 2023Leak/Splash; Gas/Air Leak; Leak/Splash; Gas/Air Leak

    IT WAS REPORTED TO VYAIRE MEDICAL THAT THE 2D0735X WATER STERILE F/INHAL FLEX 1000ML 14/CS WERE LEAKING FROM THE BOTTOM SEAM OF THE BAG WHILE CONNECTED TO A PATIENT. THERE WAS NO PATIENT HARM.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17331011 ↗

Other Humidifier, Respiratory Gas, (Direct Patient Interface) devices

All Humidifier, Respiratory Gas, (Direct Patient Interface) devices →

Sources and updates

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