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AirLife 2K8085Recalls & reported problems

Carefusion Corporation · Airlife™ Large AirLife SeeBreath CO2 Detector · Class 2

All models of AirLife (23)

Data updated Oct 16, 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 10885403185724), received between Jan 15, 2020 and Jan 15, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Sensing 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 16, 2026.

Most reported problems

Device problems

  • Device Sensing Problem1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJan 15, 2020Device Sensing Problem; Device Sensing Problem

    THE CUSTOMER REPORTED THAT THE AIRLIFE ADULT CO2 DETECTOR FAILED TO CHANGE COLOR IN THE PRESENCE OF EXHALED CO2 DURING CODE BLUE ON AN INTUBATED PATIENT. IT WAS ALSO REPORTED THAT THE TUBE WAS IN THE CORRECT POSITION. THE CUSTOMER CONFIRMED THAT THERE WAS NO PATIENT HARM ASSOCIATED WITH THE EVENT.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9593562 ↗

Other ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE devices

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Sources and updates

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