AirLife™ 124030EURecalls & reported problems
Airlife · Filtered Small Volume Nebulizer System · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10190752144828), received between Sep 5, 2020 and Jun 2, 2023 — classified as 2 injuries, 1 malfunction.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (2 reports).
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
- Patient Device Interaction Problem2
- Chemical Problem1
Patient problems
- Bronchospasm2
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJun 2, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
IT WAS REPORTED TO VYAIRE MEDICAL THAT THE PATIENT EXPERIENCE A BRONCHOSPASM AFTER USING 124030EU AIRLIFE FILTERED NEBULIZER.
Patient problems: Bronchospasm
MAUDE report 17051811 ↗InjuryJun 2, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
IT WAS REPORTED TO VYAIRE MEDICAL THAT THE PATIENT EXPERIENCED BURNING IN THE CHEST AFTER RECEIVING TREATMENT WITH AIRLIFE FILTERED SMALL VOLUME NEBULIZER SYSTEM. FURTHERMORE, THERE IS NO INFORMATION REGARDING PATIENT HARM.
Patient problems: Bronchospasm
MAUDE report 17051788 ↗MalfunctionSep 5, 2020Chemical Problem; Chemical Problem
THE CUSTOMER REPORTED THAT THE 124030EU AIRLIFE® FILTERED SMALL VOLUME NEBULIZER SYSTEM EXPERIENCED MUCH LONGER THERAPY (NEBULIZING PENTAMIDINE) THAN THEY USED TO BE. FILTER LETS THROUGH MEDICATION WHICH ARE IRRITATING FOR CLINICIAN. ALSO "WHITE SMOKE" WHICH CAME OUT OF THE FILTER THAT IRRITATED THEIR EYES AFTER TREATMENT. THE CUSTOMER CONFIRMED THAT THERE WAS NO HARM OR HAZARD OCCURRED TO THE PATIENT. THEY STILL CONTINUED EVEN THOUGH IT LOOKED LONGER AND EVEN THERE WAS EMANATIONS IN THE ROOM. NO INTERVENTION WAS DONE TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10498067 ↗
Other NEBULIZER (DIRECT PATIENT INTERFACE) devices
- HUDSON RCI IPN049807Teleflex Incorporated · NEBULIZER (DIRECT PATIENT INTERFACE)62 reports
- Circulaire™ 0330Sunmed, LLC · Nebulizer (Direct Patient Interface)1 recall0 reports
- I neb 00Respironics Respiratory Drug Delivery (Uk) Ltd · NEBULIZER (DIRECT PATIENT INTERFACE)3 deaths15 reports
- VixOne 0209Westmed, Inc. · Nebulizer (Direct Patient Interface)13 reports
- HUDSON RCI IPN040620Teleflex Incorporated · NEBULIZER (DIRECT PATIENT INTERFACE)12 reports
- HUDSON RCI HUD05014Medline Industries, Inc. · Nebulizer (direct patient interface)6 reports
- HUDSON RCI IPN049808Teleflex Incorporated · NEBULIZER (DIRECT PATIENT INTERFACE)6 reports
- VixOne 0210Westmed, Inc. · Nebulizer (Direct Patient Interface)5 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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