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Medline Industries, Inc. LYN003EYUPARecalls & reported problems

Medline Industries, Inc. · EYE PACK UPMC · 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 10193489374445), received between May 5, 2022 and May 5, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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

  • Device Contamination with Chemical or Other Material1

Patient problems

  • Foreign Body Sensation in Eye1

Recent adverse event reports

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

  • InjuryMay 5, 2022Device Contamination with Chemical or Other Material

    ACCORDING TO THE FACILITY A FIBER WAS DISCOVERED POST CATARACT PROCEDURE AND NEEDED AN ADDITIONAL PROCEDURE TO REMOVE THE FIBER.

    Patient problems: Foreign Body Sensation in Eye

    MAUDE report 14289350 ↗

Other Eye tray devices

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Sources and updates

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