AirLife 004081Recalls & reported problems
Vyaire Medical, Inc. · CONNECTOR U/ADAPIT STR 22MM ID X 22MM OD · Class 1
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10190752154193), received between Dec 14, 2023 and Nov 19, 2025 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Disconnection” (3 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Disconnection3
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 19, 2025Break; Break
IT WAS REPORTED: THE OXYGEN CONNECTOR THAT "TEE'D" INTO THE OXYGEN TO THE PATIENT'S CONTINUOUS POSITIVE AIRWAY PRESSURE (CPAP) SNAPPED OFF. THERE WAS NO APPARENT HARM TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23601288 ↗MalfunctionDec 14, 2023Disconnection; Disconnection
IT WAS REPORTED TO VYAIRE MEDICAL THAT THE 004081 CONNECTOR U/ADAPIT STR 22MM ID X 22MM OD PLUG THAT CLOSES THE OXYGEN STEM WILL NOT STAY IN PLACE. THIS ISSUE WILL LEAD TO AN UNINTENTIONAL CIRCUIT LEAK. THERE WAS NO HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18332349 ↗MalfunctionDec 14, 2023Disconnection; Disconnection
IT WAS REPORTED TO VYAIRE MEDICAL THAT THE 004081 CONNECTOR U/ADAPIT STR 22MM ID X 22MM OD PLUG THAT CLOSES THE OXYGEN STEM WILL NOT STAY IN PLACE. THIS ISSUE WILL LEAD TO AN UNINTENTIONAL CIRCUIT LEAK. THERE WAS NO HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18332326 ↗MalfunctionDec 14, 2023Disconnection; Disconnection
IT WAS REPORTED TO VYAIRE MEDICAL THAT THE 004081 CONNECTOR U/ADAPIT STR 22MM ID X 22MM OD PLUG THAT CLOSES THE OXYGEN STEM WILL NOT STAY IN PLACE. THIS ISSUE WILL LEAD TO AN UNINTENTIONAL CIRCUIT LEAK. THERE WAS NO HARM REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18331531 ↗
Other Connector, Airway (Extension) devices
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- ErgoStar CM 55 MP01855Drägerwerk AG & Co. KGaA · Connector, Airway (Extension)1 recall10 reports
- ErgoStar CM 40 MP01840Drägerwerk AG & Co. KGaA · Connector, Airway (Extension)1 recall1 report
- ErgoStar CM 45 MP01845Drägerwerk AG & Co. KGaA · Connector, Airway (Extension)1 recall1 report
- Omnistream 011401Oridion Medical 1987 Ltd. · CONNECTOR, AIRWAY (EXTENSION)1 recall0 reports
- ErgoStar CM 60 MP01860Drägerwerk AG & Co. KGaA · 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.