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Medline Industries, Inc. DYNJ81664Recalls & reported problems

Medline Industries, Inc. · CATARACT EYE PACK · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
3
Deaths reported
0
Injuries reported
3
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10195327135829), received between Aug 24, 2023 and Aug 24, 2023 — classified as 3 injuries.

The most frequently reported specific device problem is “Material Integrity Problem” (3 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 18, 2026.

Most reported problems

Device problems

  • Material Integrity Problem3

Patient problems

  • Foreign Body In Patient3

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • InjuryAug 24, 2023Material Integrity Problem; Material Integrity Problem

    WHITE THREAD IN THE SURGICAL SITE NOTED DURING FINAL SWEEP WITH MICROSCOPE.

    Patient problems: Foreign Body In Patient

    MAUDE report 17614053 ↗
  • InjuryAug 24, 2023Material Integrity Problem; Material Integrity Problem

    A WHITE THREAD WAS REMOVED FROM THE EYE FOLLOWING A PHACOEMULSIFICATION.

    Patient problems: Foreign Body In Patient

    MAUDE report 17613418 ↗
  • InjuryAug 24, 2023Material Integrity Problem; Material Integrity Problem

    THREAD HAD TO BE REMOVED FROM EYE.

    Patient problems: Foreign Body In Patient

    MAUDE report 17613000 ↗

Other Eye tray devices

All Eye tray devices →

Sources and updates

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