AirLife™ CSC100 (UDI 10889483598764)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889483598764), received between Oct 15, 2025 and Oct 15, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Patient Device Interaction 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

Recent adverse event reports

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

• MalfunctionOct 15, 2025Patient Device Interaction Problem; Patient Device Interaction Problem

  IT WAS REPORTED: THE ANXIOUS INTUBATED PATIENT, IN THE INTENSIVE CARE UNIT (ICU), PULLED THE CLOSED SUCTION CATHETER (CSC) OFF FROM THE VERSO ADAPTER. ADDITIONALLY, THE DUCK VALVE, INSIDE THE VERSO ADAPTER CSC100, FELL DOWN INTO THE SWIVEL PART OF THE DEVICE, WHERE THE STAFF DISCOVERED IT. THE SYSTEM WAS CHANGED; THERE WAS NO DIRECT IMPACT ON THE PATIENT'S CONDITION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23305971 ↗