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Medicon 09.95.92Recalls & reported problems

Medicon eG. Chirurgiemechaniker-Genossenschaft · Varady phleboextractor 18cm · 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 04046826015213), received between May 4, 2019 and May 4, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Handling 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Device Handling Problem1
  • Fracture1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionMay 4, 2019Fracture; Device Handling Problem; Fracture; Device Handling Problem

    THE DEVICE TIP BROKE OFF DURING CLINICAL USE AND WAS IMMEDIATELY REMOVED FROM THE OPERATIVE FIELD. THERE WERE NO CONSEQUENCES TO THE PATIENT.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8580692 ↗

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