BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    V. MUELLER BRUNS

    MDR report key: 1694411 · Received May 17, 2010

    Report

    Report Number
    1694411
    Event Type
    Malfunction
    Date Received
    May 17, 2010
    Date of Event
    May 17, 2010
    Report Date
    May 17, 2010
    Manufacturer
    CAREFUSION
    Product Code
    FZS
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    NC, US

    Narratives

    Description of Event or Problem · 1

    WHILE SURGEON WAS PERFORMING A LEFT KNEE ARTHROPLASTY, THE CURETTE TIP BROKE OFF. CURETTE TIP WAS RETRIEVED, THERE WAS NO HARM TO THE PATIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 V. MUELLER BRUNS CURETTE FZS CAREFUSION * *

    Patients

    Seq Age Sex Outcome Treatment
    1 41 YR