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AESCULAP FT495TRecalls & reported problems

Aesculap AG · YASARGIL XS Clip Applier Forceps, 8 3/4", (220 mm), working length: 3 1/2", (90 mm), bayonet-shaped, with ratchet, standard, titanium · Class 2

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

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04038653327447), received between Aug 9, 2023 and Aug 9, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Failure to Fire” (2 reports).

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

  • Failure to Fire2

Patient problems

  • Hemorrhage/Blood Loss/Bleeding2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryAug 9, 2023Failure to Fire; Failure to Fire

    UPDATE: THERE WAS A 5 MINUTE DELAY IN SURGERY. AN ADDITIONAL INSTRUMENT SET WAS OPENED AND A BACKUP NON-LOCKING APPLIER USED INSTEAD.

    Patient problems: Hemorrhage/Blood Loss/Bleeding

    MAUDE report 17493937 ↗
  • InjuryAug 9, 2023Failure to Fire; Failure to Fire

    INVESTIGATION COMPLETE.

    Patient problems: Hemorrhage/Blood Loss/Bleeding

    MAUDE report 17493935 ↗

Other APPLIER, ANEURYSM CLIP devices

All APPLIER, ANEURYSM CLIP devices →

Sources and updates

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