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Medline Industries, Inc. DYNJ44922FRecalls & reported problems

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

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

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 10193489338188), received between Sep 22, 2021 and Sep 22, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1

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.

  • InjurySep 22, 2021Detachment of Device or Device Component

    A PATIENT WAS UNDERGOING A TARSAL STRIP OF THE LOWER EYELID AND UPON ATTEMPTING TO INJECT THE EYELID THE 30G 1/2" NEEDLE CAME AWAY FROM THE 3ML LUER LOCK SYRINGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12514280 ↗

Other Eye tray devices

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Sources and updates

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