BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STRETCHER

    MDR report key: 2091223 · Received April 20, 2011

    Report

    Report Number
    1831750-2011-03848
    Event Type
    Malfunction
    Date Received
    April 20, 2011
    Date of Event
    March 25, 2011
    Report Date
    March 25, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD-END JACK WAS DRIFTING WITH AND WITHOUT WEIGHT APPLIED. IT IS UNK IF THERE WAS PT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRETCHER HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1010 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK