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AirLife CK0005Recalls & reported problems

Carefusion Corporation · Airlife™ Prefill Nebulizer Kit Nebulizer Cap and Sterile Water for Inhalation, USP, 500 ml · 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
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885403221477), received between Dec 7, 2020 and Dec 7, 2020 — classified as 1 injury.

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

  • Defective Device1

Patient problems

  • Nasal Obstruction1

Recent adverse event reports

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

  • InjuryDec 7, 2020Defective Device; Defective Device

    IT WAS REPORTED TO VYAIRE MEDICAL THAT OUR NEB KIT W ADAPTER STERILE WATER 500ML WAS NOT ABLE TO MIST. A PATIENT DEVELOPED A MUCOUS PLUG AND NEEDED INTERVENTIONS WITH LAVAGING AND SUCTIONING.

    Patient problems: Nasal Obstruction

    MAUDE report 10960485 ↗

Other Humidifier nebulizer kit devices

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Sources and updates

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