BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PRIME BIG WHEEL ELECT STRETCHER

    MDR report key: 2110116 · Received May 19, 2011

    Report

    Report Number
    1831750-2011-04875
    Event Type
    Malfunction
    Date Received
    May 19, 2011
    Date of Event
    April 21, 2011
    Report Date
    April 21, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    EVAL RESULT: LATCH RELEASE HANDLE.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT RIGHT SIDE RELEASE HANDLE WAS DAMAGED PRESENTING SHARP EDGES. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1