AirLife™ 603CHRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10190752155817), received between Feb 21, 2020 and Mar 2, 2020 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 2, 2020Detachment of Device or Device Component; Detachment of Device or Device Component

  THE CUSTOMER REPORTED THAT THE 9025TRU 1ML SYRINGE 25G 5/8" WHEN INSERTING INTO PATIENT'S ARM, NEEDLE DETACHES FROM THE SYRINGE. UNKNOWN PATIENT HARM REPORTED AS OF NOW.

  Patient problems: No Information

  MAUDE report 9777489 ↗
• MalfunctionFeb 21, 2020Material Integrity Problem; Material Integrity Problem

  THE CUSTOMER REPORTED AN ISSUE WITH ABG KITS. THE LUER LOCK THREADS ATTACHING THE NEEDLE TO THE SAFETY CATCH OOZES BLOOD WHILE OBTAINING AN ABG SAMPLE FROM AN (B)(6) PATIENT. AT THIS TIME, THERE IS NO INFORMATION REGARDING PATIENT HARM.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 9741633 ↗