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AirLife™ AH180Recalls & reported problems

Airlife · AirLife™ Adult Heated Wire Circuit, Dual-limb, Dual-heated circuit · Class 2

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 10190752145146), received between Oct 28, 2021 and Oct 28, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Moisture or Humidity Problem” (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

  • Moisture or Humidity Problem1

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.

  • MalfunctionOct 28, 2021Moisture or Humidity Problem; Moisture or Humidity Problem

    THE CUSTOMER REPORTED THAT THE AIRLIFE¿ ADULT HEATED WIRE CIRCUIT DUAL-LIMB, DUAL-HEATED CIRCUIT EXPERIENCED CIRCUITS BECAME FLOODED WITH WATER. THE CUSTOMER CONFIRMED THAT THERE WAS NO PATIENT HARM ASSOCIATED WITH THE REPORTED EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12715860 ↗

Other HEATER, BREATHING SYSTEM W/WO CONTROLLER (NOT HUMIDIFIER OR NEBULIZER devices

All HEATER, BREATHING SYSTEM W/WO CONTROLLER (NOT HUMIDIFIER OR NEBULIZER devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.