BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 56704 · Received October 3, 1996

    Report

    Report Number
    1920664-1996-00684
    Event Type
    Malfunction
    Date Received
    October 3, 1996
    Date of Event
    August 29, 1996
    Product Code
    HQC
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    THE PHACOEMULSIFICATION HANDPIECE WAS NOT RETURNED FOR EVALUATION AGAINST THIS MEDWATCH. IT WAS INVOLVED IN ADD'L INCIDENTS AND SUBSEQUENTLY REPORTED UNDER MEDWATCH 1920664-1996-851, 1920664-1996-852 AND 1920664-1996-853. EVALUATION OF HANDPIECE CAN BE FOUND AS FOLLOW-UP TO THE SUBSEQUENT MEDWATCH REPORTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * HQC

    Patients

    Seq Age Sex Outcome Treatment
    1 *