AirLife™ 9025TRURecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10190752155084), received between May 13, 2021 and Oct 1, 2021 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Defective Component” (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 18, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 1, 2021Mechanical Problem; Mechanical Problem

  THE CUSTOMER REPORTED THAT THE AIRLIFE® ARTERIAL BLOOD SAMPLER EXPERIENCED NOT PUMPING UP. THE CUSTOMER CONFIRMED THAT THERE WAS NO PATIENT HARM ASSOCIATED WITH THE REPORTED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12561422 ↗
• MalfunctionSep 20, 2021Use of Device Problem; Use of Device Problem

  THE CUSTOMER REPORTED THAT THE AIRLIFE® ARTERIAL BLOOD SAMPLER EXPERIENCED BLOOD DOES NOT FLOW UP THE SYRINGES AS IF THERE IS ADDITIONAL BACK PRESSURE. BLOOD IS FLASHING IN THE HUB THEN FLOWING BACK TO THE PATIENT. THE CUSTOMER CONFIRMED THAT THERE WAS NO PATIENT HARM ASSOCIATED WITH THE REPORTED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12502521 ↗
• MalfunctionJul 8, 2021Filling Problem; Filling Problem

  THE CUSTOMER REPORTED THAT DURING THE ARTERIAL SAMPLING, THE BLOOD DOES NOT RISE AS USUAL BUT THERE IS A DRAUGHT WITH BUBBLES, THERE IS BLOOD DRIPPING FROM THE SYRINGE WHEN ASPIRATING, AND ALSO, THE TIP OF THE SYRINGE, WHICH USUALLY FITS THE OPTI CASSETTE PERFECTLY, IS NOW TOO THIN, SO THE SYRINGE DOESN'T FIT WELL ON THE CASSETTE. THERE WAS NO PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12136053 ↗
• MalfunctionMay 13, 2021Defective Component; Defective Component

  THE CUSTOMER REPORTED THAT THE AIRLIFE® ARTERIAL BLOOD SAMPLER EXPERIENCED PLUNGER IN THE SYRINGE IS NOT WORKING. THE CUSTOMER CONFIRMED THAT THERE WAS NO PATIENT HARM ASSOCIATED WITH THE REPORTED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11816349 ↗