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Alcon, Coherent 8065750133Recalls & reported problems

Alcon Laboratories, Inc. · 25 GA Straight Laser Probe · Class 2

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 00380657501335), received between Nov 19, 2021 and Nov 19, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fitting 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

  • Fitting Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionNov 19, 2021Fitting Problem; Fitting Problem

    A HEALTH PROFESSIONAL REPORTED THAT DURING A VITREO-RETINAL SURGERY, AN OPHTHALMIC LASER PROBE WOULD NOT FIT PROPERLY INTO THE TROCAR. AN ALTERNATE LASER PROBE WAS OBTAINED IN ORDER TO COMPLETE THE PROCEDURE. THERE WAS NO HARM TO THE PATIENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12846006 ↗

Other Instrument, vitreous aspiration and cutting, ac-powered devices

All Instrument, vitreous aspiration and cutting, ac-powered devices →

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