Skip to content

GIBECK IPN043834Recalls & reported problems

Teleflex Incorporated · HUMID VENT FILTER LIGHT S · Class 1

All models of GIBECK (7)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04026704388745), received between Jan 4, 2022 and Jan 4, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Contamination /Decontamination 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

Device problems

  • Contamination /Decontamination Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionJan 4, 2022Contamination /Decontamination Problem; Contamination /Decontamination Problem

    IT WAS REPORTED "A THERAPIST PLACED A NEW HUMID VENT FILTER ON A PATIENT, HEARD RATTLING, REMOVED AND SHOOK IT WITH LARGE AMOUNT OF WHITE PARTICLES FLYING EVERYWHERE". NO PATIENT INJURY OR HARM REPORTED. PATIENT CONDITION REPORTED AS "FINE".

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13151122 ↗

Other CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE) devices

All CONDENSER, HEAT AND MOISTURE (ARTIFICIAL NOSE) devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page