BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RESISTANCE 29

    MDR report key: 2914878 · Received December 7, 2012

    Report

    Report Number
    1831750-2012-12626
    Event Type
    Malfunction
    Date Received
    December 7, 2012
    Date of Event
    November 8, 2012
    Report Date
    November 8, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THE FOOT END BRAKES WOULD NOT HOLD. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RESISTANCE 29 HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1711 NA

    Patients

    Seq Age Sex Outcome Treatment
    1