BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PRIMEBIG WHEEL ELECT STRETCHER

    MDR report key: 2890558 · Received November 9, 2012

    Report

    Report Number
    1831750-2012-11747
    Event Type
    Malfunction
    Date Received
    November 9, 2012
    Date of Event
    October 13, 2012
    Report Date
    October 13, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    GROUND PRONG.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE GROUND PRONG WAS MISSING FROM THE POWER CORD. THE CUSTOMER REPORTED THAT THEY DID NOT KNOW IF THERE WAS PATIENT INVOLVEMENT OR IF THERE WERE ADVERSE CONSEQUENCES TO REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PRIMEBIG WHEEL ELECT STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1115000000E NA

    Patients

    Seq Age Sex Outcome Treatment
    1