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AESCULAP FT740TRecalls & reported problems

Aesculap AG · YASARGIL TI PERM STD-CLIP STR 7MM · Class 2 · Implant

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04038653171460), received between Nov 16, 2021 and Nov 16, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Migration or Expulsion of Device” (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

  • Migration or Expulsion of Device1

Patient problems

  • Failure of Implant1

Recent adverse event reports

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

  • InjuryNov 16, 2021Migration or Expulsion of Device; Migration or Expulsion of Device

    CLARIFICATION: A WEEK POSTOPERATIVELY, THE POSITION OF THE CLIP HAD BEEN DEVIATED A FEW MM DISTALLY FROM THE ANEURYSM NECK AND THE POSITION OF THE INITIAL CLIP CLOSURE. APPROXIMATELY 2 WEEKS AFTER THE PRODUCT WAS USED (CLOSED) BY CLIPPING, THE CLIP SLIPPED OUT AND RE-RUPTURE OCCURRED AT THE SAME SITE. CURRENTLY, THE REVISION PROCEDURE HAS BEEN COMPLETED.

    Patient problems: Failure of Implant

    MAUDE report 12821381 ↗

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.