BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STAIR PRO- MODEL 6252

    MDR report key: 2935471 · Received January 4, 2013

    Report

    Report Number
    1831750-2013-90119
    Event Type
    Malfunction
    Date Received
    January 4, 2013
    Date of Event
    December 13, 2012
    Report Date
    December 13, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPP
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    LOCK BAR STRUT.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE LOCK BAR STRUT WAS BROKEN ON THE STAIR CHAIR. THERE WAS PATIENT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    5731 STAIR PRO- MODEL 6252 STRETCHER, HAND-CARRIED FPP STRYKER MEDICAL 6252 NA

    Patients

    Seq Age Sex Outcome Treatment
    1