AirLife™ T64CRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10190752145566), received between Feb 28, 2020 and Feb 28, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Decrease in Suction” (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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 28, 2020Decrease in Suction; Decrease in Suction

  THE CUSTOMER REPORTED THAT THE AIRLIFE TRI-FLO SUCTION CATHETER ARE NOT EVEN HOLLOWED OUT PROPERLY TO BE ABLE TO CREATE SUCTION. THE ISSUE OCCUR WHILE USE ON A (B)(6)-YEAR-OLD TRACHEOSTOMY AND GASTROSTOMY TUBE DEPENDENT PATIENT WHICH ALMOST TAKEN SALINE INTO HIS LUNGS. THE CUSTOMER CONFIRMED THAT THERE WAS NO PATIENT HARM.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9772030 ↗