BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MEDLINE

    MDR report key: 24801583 · Received April 7, 2026

    Report

    Report Number
    1423395-2026-00080
    Event Type
    Injury
    Date Received
    April 7, 2026
    Date of Event
    March 11, 2026
    Report Date
    April 7, 2026
    Manufacturer
    MEDLINE INDUSTRIES LP
    Product Code
    OJK
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    ACCORDING TO THE CUSTOMER, "CORNEAL ABRASIONS" WERE REPORTED RELATED TO THE DRAPE IN THE PACK. NO ADDITIONAL DETAILS ARE AVAILABLE RELATED TO THE CUSTOMER REPORTED ISSUE. DESPITE MULTIPLE GOOD FAITH EFFORTS TO OBTAIN ADDITIONAL INFORMATION, THE CUSTOMER CONTACT WAS UNABLE OR UNWILLING TO PROVIDE FURTHER INCIDENT DETAILS TO THE MANUFACTURER. NO ADDITIONAL INFORMATION IS AVAILABLE. IT HAS BEEN DETERMINED THAT THE REPORTED EVENT CAUSED OR CONTRIBUTED TO SERIOUS INJURY, THEREFORE, THIS MEDWATCH IS BEING FILED. IF ANY FURTHER RELEVANT INFORMATION IS IDENTIFIED OR OBTAINED, A SUPPLEMENTAL MEDWATCH WILL BE SUBMITTED.

    Description of Event or Problem · 0

    CORNEAL ABRASIONS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    60676 MEDLINE GLAUCOMA PACK-LF OJK MEDLINE INDUSTRIES LP

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other