AirLife™ 004083Recalls & reported problems
Vyaire Medical, Inc. · U/Adapt-It Straight Adapter · Class 1
All models of AirLife (25)
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 10190752152595), received between Mar 23, 2024 and Mar 23, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Connection 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.
Reports received per month
Most reported problems
Device problems
- Connection Problem1
- Incomplete or Inadequate Connection1
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.
MalfunctionMar 23, 2024Connection Problem; Incomplete or Inadequate Connection; Connection Problem; Incomplete or Inadequate Connection
THE PLASTIC CAP THAT IS ATTACHED DOES NOT STAY CLOSED AND POPS OPEN WITH ANY BREATH DELIVERED BY THE VENTILATOR. REPORT INDICATES THIS IS ADVERSE EVENT, BUT DOES NOT INDICATE ADVERSE EFFECT ON THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18965559 ↗
Other CONNECTOR, AIRWAY (EXTENSION) devices
- Flex Extenders 7-5132Westmed, Inc. · Connector, Airway (Extension)1 recall18 reports
- ErgoStar CM 55 MP01855Drägerwerk AG & Co. KGaA · Connector, Airway (Extension)1 recall10 reports
- ErgoStar CM 45 MP01845Drägerwerk AG & Co. KGaA · Connector, Airway (Extension)1 recall1 report
- ErgoStar CM 40 MP01840Drägerwerk AG & Co. KGaA · Connector, Airway (Extension)1 recall1 report
- ErgoStar CM 60 MP01860Drägerwerk AG & Co. KGaA · Connector, Airway (Extension)1 recall0 reports
- Omnistream 011401Oridion Medical 1987 Ltd. · CONNECTOR, AIRWAY (EXTENSION)1 recall0 reports
- Adaptors/Connectors S6411PWestmed, Inc. · Connector, Airway (Extension)1 recall0 reports
- Portex 66-1991Icu Medical, Inc. · CONNECTOR, AIRWAY (EXTENSION)8 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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