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AirLife™ AH132Recalls & reported problems

Airlife · AirLife™ Infant Single Limb Heated Wire Circuit Kit Single-limb, Single-heated, continuous-flow circuit (>4 L/min) Contains AH032 Circuit, AH290 Chamber · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10190752145122), received between May 10, 2023 and May 10, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Temperature 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Temperature 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.

  • InjuryMay 10, 2023Temperature Problem; Temperature Problem

    IT WAS REPORTED TO VYAIRE MEDICAL THAT THE HUMIDIFIER WAS NOT HEATING DUE TO A BENT PRONG ON AIRLIFE¿ INFANT SINGLE LIMB HEATED WIRE CIRCUIT KIT.THE REPORTED ISSUE OCCURRED DURING PATIENT USE AND THE CIRCUIT WAS CHANGED. THE CUSTOMER CONFIRMED THAT THERE WAS NO PATIENT HARM ASSOCIATED WITH THE REPORTED EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16908551 ↗

Other Anesthesia breathing circuit kit (adult & pediatric) devices

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Sources and updates

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