BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSPORT SERIES OBS10/25/04

    MDR report key: 3002741 · Received March 13, 2013

    Report

    Report Number
    0001831750-2013-02003
    Event Type
    Malfunction
    Date Received
    March 13, 2013
    Date of Event
    February 15, 2013
    Report Date
    February 15, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE CUSTOMER ALLEGED THAT THE CASTER WAS DAMAGED, POSSIBLY RESULTING IN REDUCED BRAKING FORCE. NO IMPACT TO THE BRAKE ASSEMBLY WAS REPORTED AND NO DAMAGE TO THE OTHER THREE CASTERS WAS REPORTED. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    105239 TRANSPORT SERIES OBS10/25/04 STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO 0721

    Patients

    Seq Age Sex Outcome Treatment
    1