BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SM104 M-SERIES W/5TH WHEEL

    MDR report key: 757180 · Received August 25, 2006

    Report

    Report Number
    1831750-2006-00052
    Event Type
    Injury
    Date Received
    August 25, 2006
    Date of Event
    July 28, 2006
    Report Date
    July 28, 2006
    Manufacturer
    STRYKER CORP, MED. DIV.
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    IN ORDER FOR THE LITTER SURFACE TO LOWER, THE DESCENT PEDAL MUST BE DEPRESSED AND REMAIN DEPRESSED FOR THE UNIT TO CONTINUE TO LOWER. THE MOMEMT THE DESCENT PEDAL IS NO LONGER BEING THE DEPRESSED, THE LITTER SURFACE CEASES TO LOWER.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A VISITOR IN AN ER TREATMENT ROOM AT THE FACILITY HAD THEIR LEGS RESTING ON THE BASE OF A STRETCHER. REPORTEDLY, THE VISITOR DEPRESSED THE RELEASE PEDAL CAUSING THE PATIENT SURFACE TO LOWER ONTO THE VISITOR'S LEFT LEG CAUSING A JOINT DIFFUSION OF THE LEFT FOOT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SM104 M-SERIES W/5TH WHEEL WHEELED STRETCHER FPO STRYKER CORP, MED. DIV. 1005 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Required Intervention