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HUDSON RCI IPN049856Recalls & reported problems

Teleflex Incorporated · CATH-GUIDE® AIRWAY 100 mm, No. 10 · Class 1

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 14026704646491), received between Jul 29, 2021 and Jul 29, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Complete Blockage” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Complete Blockage1

Patient problems

  • Obstruction/Occlusion1

Recent adverse event reports

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

  • MalfunctionJul 29, 2021Complete Blockage; Complete Blockage

    IT WAS REPORTED THAT "WHEN THE DOCTOR INTUBATED THE PATIENT TO SUCK SPUTUM, HE FOUND THAT THE RESISTANCE IN THE CAVITY WAS LARGE, AND IT WAS DIFFICULT TO INSERT THE SUCTION TUBE. NO IMPACT ON PATIENT". NO INJURY OR HARM REPORTED. PATIENT CONDITION REPORTED AS "FINE".

    Patient problems: Obstruction/Occlusion

    MAUDE report 12245753 ↗

Other AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY devices

All AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.