BEUDAMED
    FDA Adverse Event Summary report: N

    JAC

    MDR report key: 757448 · Received July 28, 2006

    Report

    Report Number
    MW4004200
    Date Received
    July 28, 2006
    Report Date
    June 30, 2006
    Manufacturer
    *
    Product Code
    IPR
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    THE COMPLAINT STATED THAT IF YOU USED THE CRUTCHES FOR MORE THAN 50 FEET, BLOOD BLISTERS WOULD FORM ON THE OUTSIDE OF THE THUMB AND INDEX FINGERS. THE COMPLAINANT ALLEGES THAT THE CRUTCHES ARE POORLY MANUFACTURED. THE CORNER IN WHICH THE COMPLAINANT'S HANDS WERE RUBBING AGAINST WAS A SHARP SURFACE WHICH RESULTED IN INJURY TO HIS HANDS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 JAC CRUTCH IPR * * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *