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DURAVENT 11201-07Recalls & reported problems

Andreas Fahl Medizintechnik-Vertrieb GmbH · DURAVENT XL 1 IC, SIZE 7 · Class 2

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04051948006759), received between Feb 14, 2017 and Feb 14, 2017 — classified as 1 death.

The most frequently reported specific device problem is “Detachment Of 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 16, 2026.

Most reported problems

Device problems

  • Detachment Of Device Component1

Patient problems

  • Death1

Recent adverse event reports

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

  • DeathFeb 14, 2017Detachment Of Device Component

    ANDREAS FAHL MEDIZINTECHNIK - VERTRIEB (B)(4) RECEIVED THE INFORMATION THAT A TRACHEOSTOMY TUBE BECAME DETACHED OF THE NECK PLATE WHILE PATIENT ATTEMPTED TO EXCHANGE THE INNER CANNULA. IT WAS ALLEGED THAT AFTER HAVING REMOVED THE ENTIRE CANNULA THE PATIENT PASSED AWAY.

    Patient problems: Death

    MAUDE report 6328901 ↗

Other Tube, Tracheal (W/Wo Connector) devices

All Tube, Tracheal (W/Wo Connector) devices →

Sources and updates

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