AirLife™ 441HRecalls & reported problems
Airlife · AirLife™ Nebulizer Adapter · 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 10190752131910), received between Jan 15, 2020 and Jan 15, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Disconnection” (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
- Disconnection1
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.
InjuryJan 15, 2020Disconnection; Disconnection
THE CUSTOMER REPORTED THAT THE AIRLIFE HIGH FLOW FIO2 NEBULIZER'S THREADED CONNECTION FELL OFF AND DISCONNECTED FROM THE WALL. THE EVENT OCCURRED WHILE CONNECTED TO A PATIENT. THE CUSTOMER REPORTED THAT THEY HAD REPLACED THE ADAPTER AND PLACED THE PATIENT ON A NON-RE-BREATHING OXYGEN MASK AND CONFIRMED THAT NO PATIENT HARM WAS ASSOCIATED ON THIS EVENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9593752 ↗
Other NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER) devices
- LMA ATOMIZATION IPN915303Teleflex Incorporated · NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER)18 reports
- LMA ATOMIZATION IPN048826Teleflex Incorporated · NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER)11 reports
- Salter AIRE Elite 8350-8900Salter Labs · NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER)8 reports
- Salter AIRE Elite SO-1774BESalter Labs · NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER)7 reports
- N/A 8904-7Salter Labs · NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER)5 reports
- LMA ATOMIZATION IPN049182Teleflex Incorporated · NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER)1 report
- HUDSON RCI IPN049826Teleflex Incorporated · NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER)1 report
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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