BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HERRICK LACRIMAL PLUG

    MDR report key: 376282 · Received February 8, 2002

    Report

    Report Number
    2024818-2002-00001
    Event Type
    Injury
    Date Received
    February 8, 2002
    Date of Event
    January 1, 2001
    Report Date
    January 28, 2002
    Manufacturer
    LACRIMEDICS, INC.
    Product Code
    LZU
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    HERRICK PLUG ALLEGEDLY EMBEDDED IN CANALICULUS REQUIRING A SURGICAL PROCEDURE (I.E. DCR) TO REMOVE. OCULOPLAST ATTEMPTED TO REMOVE PLUG(S) WITH PRESSURE IRRIGATION PRIOR TO SURGERY WITHOUT APPARENT SUCCESS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HERRICK LACRIMAL PLUG INTRACANALICULAR LACRIMAL PLUG LZU LACRIMEDICS, INC. HLP UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention