BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LARGE DIAMETER LACRIMAL INTUBATION SET/STENTUBE

    MDR report key: 703071 · Received April 12, 2006

    Report

    Report Number
    1649914-2006-00023
    Event Type
    Malfunction
    Date Received
    April 12, 2006
    Report Date
    March 30, 2006
    Manufacturer
    QUEST MEDICAL, INC.
    Product Code
    HNW
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    THE LARGE STENTTUBES CAUSE "CHEES-WIRING OF THE PUNCTUM AND CANALICULUS TOO FREQUENTLY" AND THINKS THEY ARE "TOO TIGHT". THE PRODUCT WAS NOT SAVED FOR EVALUATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LARGE DIAMETER LACRIMAL INTUBATION SET/STENTUBE MANUAL OPHTHALMIC SURGICAL INSTRUMENT: LACRYMAL PROBE HNW QUEST MEDICAL, INC. LIS052 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN