BEUDAMED
    FDA Adverse Event Other Summary report: N

    7.5MM TI FLEXIBLE HUMERAL NAIL

    MDR report key: 361776 · Received November 20, 2001

    Report

    Report Number
    2520274-2001-00060
    Event Type
    Other
    Date Received
    November 20, 2001
    Date of Event
    October 31, 2001
    Report Date
    November 19, 2001
    Manufacturer
    SYNTHES (USA)
    Product Code
    JDS
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    THE SALES CONSULTANT REPORTED THAT DR. FROM HOSP COMPLAINED THAT HE NOTED A 7.5MM TI FLEXIBLE HUMERAL NAIL IS BENT AND REMAINS IN THE PT. THERE ARE NO PLANS FOR REMOVAL. THE PT IS HEALING VERY WELL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    52507 7.5MM TI FLEXIBLE HUMERAL NAIL TITANIUM INTRAMEDULLARY NAILS JDS SYNTHES (USA) NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO