AirLife™ Volume Ventilator Circuit 1.6 m (5') 001795Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10190752144729), received between Aug 7, 2020 and Nov 27, 2023 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Defective Component” (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

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 27, 2023Defective Component; Defective Component

  IT WAS REPORTED TO VYAIRE MEDICAL THAT THE 001795 CIRCUIT VENT VOL F/PORT 10/CS IS FAULTY DURING PATIENT USE. THE CUSTOMER CONFIRMED NO HARM WAS DONE TO THE PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18209890 ↗
• MalfunctionMar 18, 2021Inadequacy of Device Shape and/or Size; Inadequacy of Device Shape and/or Size

  IT WAS REPORTED TO VYAIRE MEDICAL THAT THE EXHALATION CLEAR TUBING DIAMETER IS THINNER, WHICH IS CAUSING A COLLAPSE WHILE SITTING UP IN BED AND THEY CONFIRMED THAT THE PATIENT IS NOT RECEIVING A FULL BREATH. AT THIS TIME, THERE IS NO INFORMATION REGARDING PATIENT HARM ASSOCIATED WITH THE REPORTED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11517184 ↗
• MalfunctionAug 7, 2020Defective Device; Defective Device

  THE CUSTOMER REPORTED THAT THE 001795 CIRCUIT VENT VOL F/PORT 10/CS EXPERIENCED TWO (2) TRANSPORT CIRCUITS CAUSED PATIENT VENTILATOR TO ALARM WITH PROXY LINE CHECK CIRCUIT CODE. AT THIS TIME, THERE IS NO INFORMATION REGARDING PATIENT INVOLVEMENT ASSOCIATED WITH THE REPORTED EVENT.

  Patient problems: No Information

  MAUDE report 10382897 ↗