AirLife™ 001302Recalls & reported problems
Vyaire Medical, Inc. · AirLife™ Oxygen Tubing 7 feet (2.1 m) Crush Resistant Oxygen Tubing, Vinyl Tipped · Class 1
All models of AirLife (25)
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 10190752116603), received between Mar 6, 2020 and Dec 23, 2020 — classified as 2 injuries, 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.
Most reported problems
Device problems
- Connection Problem1
- Leak/Splash1
- Loose or Intermittent Connection1
Patient problems
- No Known Impact Or Consequence To Patient2
- Bradycardia1
- Low Oxygen Saturation1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 23, 2020Connection Problem; Connection Problem
THE CUSTOMER REPORTED THAT THE TUBING 7FT O2 VINYL TIP CRUSH 50/CS, DURING EMERGENCY, SINCE THE CHILD WHO WAS BRADYCARDIC AND DESATURATED NEEDED TO USE THE DEVICE. UPON OPENING THE O2 MANOMETER, THE TUBING BECAME LOOSE, THUS DELAYING THE INTERVENTION ON THE CHILD.
Patient problems: Bradycardia; Low Oxygen Saturation
MAUDE report 11069599 ↗InjuryJun 15, 2020Loose or Intermittent Connection; Loose or Intermittent Connection
THE CUSTOMER REPORTED THAT THE AIRLIFE OXYGEN TUBING 7' (2.1M) CRUSH RESISTANT OXYGEN TUBING, VINYL TIPPED KEEPS GETTING DISCONNECTED FROM THE HOSE NIPPLE OF THE FLOWMETER WHILE CONNECTED TO THE PATIENT VIA BAG VALVE MASK. THE END USER HAD TO PICK UP THE END OF THE TUBING AND REATTACH IT TO THE NIPPLE HOSE BEFORE IT CAN BE USED. AT THIS TIME, THERE IS NO INFORMATION REGARDING PATIENT HARM ASSOCIATED WITH THE REPORTED EVENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10155971 ↗InjuryMar 6, 2020Leak/Splash; Leak/Splash
THE CUSTOMER REPORTED THAT THE AIRLIFE OXYGEN TUBING IS LEAKING AT THE SAME CONNECTION SITE AS THE GREEN CUFF, WHERE THE TUBING INITIALLY MEETS THE CUFF SITE OXYGEN WAS LEAKING PROFUSELY. THIS ISSUE OCCURRED WHILE CONNECTED TO A PATIENT AND THE TUBE WAS REPLACED WITH A NEW SET.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9802133 ↗
Other CANNULA, NASAL, OXYGEN devices
- Fisher & Paykel Healthcare OPT844Fisher & Paykel Healthcare Limited · Cannula, Nasal, Oxygen39 reports
- Fisher and Paykel Healthcare OPT312Fisher & Paykel Healthcare Limited · Cannula, Nasal, Oxygen22 reports
- Fisher and Paykel Healthcare OPT314Fisher & Paykel Healthcare Limited · Cannula, Nasal, Oxygen17 reports
- O2 Cannula 001366Salter Labs · Cannula, Nasal, Oxygen10 reports
- O2 Cannula 001365Salter Labs · Cannula, Nasal, Oxygen9 reports
- N/A 16SOFT-4Salter Labs · CANNULA, NASAL, OXYGEN8 reports
- N/A 1053-7Salter Labs · CANNULA, NASAL, OXYGEN8 reports
- Fisher & Paykel Healthcare OPT842Fisher & Paykel Healthcare Limited · Cannula, Nasal, Oxygen7 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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