AirLife™ T63CRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10190752145559), received between Mar 10, 2023 and Mar 10, 2023 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Connection 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 10, 2023Connection Problem; Connection Problem

  IT WAS REPORTED TO VYAIRE MEDICAL THE END OF THE T63C CATHETER SUCT COIL 5-6FR CONT GRAD 50/CS DOES NOT SNUGLY FIT INTO SUCTION TUBING - THERE IS NO LONGER A RIBBED CONNECTION AND THE CUSTOMER WAS UNABLE TO GET EFFICIENT SEAL TO REACH SET SUCTION PRESSURES. IT WAS USED ON A PATIENT, BUT THERE IS NO HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16525583 ↗
• MalfunctionMar 10, 2023Connection Problem; Connection Problem

  IT WAS REPORTED TO VYAIRE MEDICAL THE END OF THE T63C CATHETER SUCT COIL 5-6FR CONT GRAD 50/CS DOES NOT SNUGGLY FIT INTO SUCTION TUBING - THERE IS NO LONGER A RIBBED CONNECTION AND THE CUSTOMER WAS UNABLE TO GET EFFICIENT SEAL TO REACH SET SUCTION PRESSURES. IT WAS USED ON A PATIENT, BUT THERE IS NO HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16525264 ↗