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Constellation 8065752151Recalls & reported problems

Alcon Laboratories, Inc. · 25GA Infustion Cannula w/ Tray · 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 00380657521517), received between Apr 1, 2021 and Apr 1, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Separation” (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

  • Material Separation1

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.

  • MalfunctionApr 1, 2021Material Separation; Material Separation

    A SURGEON REPORTED THE SILVER PART OF INFUSION CANNULA TIP WAS FOUND BENT DURING SURGERY AND IT CAUSED AN IRRIGATION FAILURE DURING A CATARACT/VITRECTOMY PROCEDURE. THE PROCEDURE WAS COMPLETED AFTER REPLACING THE PRODUCT WITH ANOTHER ONE. THERE WAS NO HARM TO THE PATIENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11603318 ↗

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.