BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OEM STRETCHER

    MDR report key: 2051440 · Received April 4, 2011

    Report

    Report Number
    1831750-2011-03263
    Event Type
    Malfunction
    Date Received
    April 4, 2011
    Date of Event
    March 14, 2011
    Report Date
    March 14, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Removal / Correction Number
    Z-222-08
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BRAKES ARE BROKEN. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OEM STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 0722 NA

    Patients

    Seq Age Sex Outcome Treatment
    1