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AESCULAP FT599TRecalls & reported problems

Aesculap AG · YASARGIL TI PERM CLIP 3.5MM FEN 5/10.1 · Class 2 · Implant

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 04038653171057), received between Sep 1, 2020 and Sep 1, 2020 — classified as 1 malfunction.

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

Most reported problems

Device problems

  • Defective Component1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionSep 1, 2020Defective Component; Defective Component

    IT WAS REPORTED THAT THERE WAS AN ISSUE WITH A YASARGIL PERMANENT CLIP. ACCORDING TO THE COMPLAINT DESCRIPTION DURING SURGERY ABSCENCE OF PRESSURE WAS NOTED. THERE WAS NO PATIENT HARM. ADDITIONAL INFORMATION WAS NOT PROVIDED NOR AVAILABLE. THE MALFUNCTION IS FILED UNDER AAG REFERENCE (B)(4).

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 10480217 ↗

Other CLIP, ANEURYSM devices

All CLIP, ANEURYSM devices →

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