BEUDAMED
    FDA Adverse Event Death Summary report: N

    UNKNOWN_MEDICAL_PRODUCT

    MDR report key: 3206468 · Received July 3, 2013

    Report

    Report Number
    0001831750-2013-06083
    Event Type
    Death
    Date Received
    July 3, 2013
    Date of Event
    June 6, 2013
    Report Date
    June 7, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    PRODUCT CODE: FPO. COMMON DEVICE NAME: STRETCHER, WHEELED.

    Description of Event or Problem · 1

    AMBULANCE THAT WAS INVOLVED IN A VEHICLE COLLISION IN WHICH RESULTED IN THE DEATH OF BOTH PARAMEDICS AND THE PATIENT THAT WAS BEING TRANSPORTED. NO FURTHER INFORMATION REGARDING THIS INCIDENT HAS BEEN PROVIDED AT THIS TIME. NO REPORTED PRODUCT MALFUNCTION AT THIS TIME. MANUFACTURES INVESTIGATION IS ONGOING. IF ADDITIONAL INFORMATION IS RECEIVED A FOLLOW UP REPORT MAY BE ISSUED.

    Description of Event or Problem · 1

    AMBULANCE THAT WAS INVOLVED IN A VEHICLE COLLISION IN WHICH RESULTED IN THE DEATH OF BOTH PARAMEDICS AND THE PATIENT THAT WAS BEING TRANSPORTED. NO FURTHER INFORMATION REGARDING THIS INCIDENT HAS BEEN PROVIDED AT THIS TIME. NO REPORTED PRODUCT MALFUNCTION AT THIS TIME. MANUFACTURES INVESTIGATION IS ONGOING. IF ADDITIONAL INFORMATION IS RECEIVED A FOLLOW UP REPORT MAY BE ISSUED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    303940 UNKNOWN_MEDICAL_PRODUCT STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1 Death