BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    WECK HEM-O-LOK CLIPS MED

    MDR report key: 1860234 · Received September 22, 2010

    Report

    Report Number
    3003898360-2010-00422
    Event Type
    Malfunction
    Date Received
    September 22, 2010
    Date of Event
    September 2, 2010
    Report Date
    September 3, 2010
    Manufacturer
    TELEFLEX MEDICAL
    Product Code
    FZP
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    PRODUCT HAS NOT YET BEEN RECEIVED BY MANUFACTURER; THEREFORE, INVESTIGATION REPORT IS INCOMPLETE AT THIS TIME. A FOLLOW-UP INVESTIGATION REPORT WILL BE SENT WHEN COMPLETED.

    Description of Event or Problem · 1

    THE EVENT IS REPORTED AS: CLIPS DO NOT CLOSE WHEN THEY ARE IMPLEMENTED ON THE PATIENT. NO INJURIES REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 WECK HEM-O-LOK CLIPS MED HEM-O-LOK CLIPS FZP TELEFLEX MEDICAL NA 01H0800236

    Patients

    Seq Age Sex Outcome Treatment
    1