BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CAPTUS 3000 UPTAKE PROBE

    MDR report key: 3525152 · Received December 13, 2013

    Report

    Report Number
    MW5033476
    Event Type
    Injury
    Date Received
    December 13, 2013
    Date of Event
    December 11, 2013
    Report Date
    December 12, 2013
    Manufacturer
    CAPINTEC. INC.
    Product Code
    IZD
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    THE TECH IN NUCLEAR MEDICINE WAS POSITIONING THE UPTAKE PROBE TO TAKE A COUNT DURING A THYROID SCAN. THE PROBE WAS OVER THE PT'S LEG WHEN THE PROBE FELL ON THE PT'S LEFT KNEE. THE PT STATED SHE HAD 6/10 LEFT KNEE AFTER THE INCIDENT. THE PT WAS ABLE TO WALK AND BEAR WEIGHT AFTERWARDS. ICE WAS PROVIDED IMMEDIATELY AND THE PT WAS TAKEN TO THE ED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    653200 CAPTUS 3000 UPTAKE PROBE CAPTUS IZD CAPINTEC. INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 71 YR Required Intervention