BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OEM STRETCHER CONFIGURATIONS

    MDR report key: 1811494 · Received August 17, 2010

    Report

    Report Number
    1831750-2010-01842
    Event Type
    Malfunction
    Date Received
    August 17, 2010
    Date of Event
    July 19, 2010
    Report Date
    July 19, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIVISION
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT MODEL 722, SERIAL # (B)(4) HAD HYDRAULIC FAILURE AFTER FIRST TIME USE.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 NA