BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PRIME ZOOM STRETCHER,30"LITTER

    MDR report key: 2931933 · Received January 28, 2013

    Report

    Report Number
    0001831750-2013-00459
    Event Type
    Malfunction
    Date Received
    January 28, 2013
    Date of Event
    January 8, 2013
    Report Date
    January 8, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    INK
    PMA / PMN Number
    K022309
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE PREVIOUS MDR INITIAL REPORT WAS SENT WITHOUT THE PMA/510(K)#. (B)(4).

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE CUSTOMER ALLEGED THAT THE STRETCHER WOULD NOT LOWER AND THE JACK WAS STUCK RAISED.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE CUSTOMER ALLEGED THAT THE STRETCHER WOULD NOT LOWER AND THE JACK WAS STUCK RAISED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    38068 PRIME ZOOM STRETCHER,30"LITTER POWERED, STRETCHER, WHEELED INK STRYKER MEDICAL-KALAMAZOO 1125000030

    Patients

    Seq Age Sex Outcome Treatment
    1