BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ADVANTAGE SERIES 26 OBS 10/04

    MDR report key: 3252867 · Received July 29, 2013

    Report

    Report Number
    0001831750-2013-06748
    Event Type
    Malfunction
    Date Received
    July 29, 2013
    Date of Event
    July 2, 2013
    Report Date
    July 3, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    DEVICE EVALUATED BUT NOT YET REPAIRED.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SIDERAIL COULD NOT REMAIN LATCHED IN PLACE. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    353742 ADVANTAGE SERIES 26 OBS 10/04 STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO 1001

    Patients

    Seq Age Sex Outcome Treatment
    1