BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STAIR PRO - MODEL 6252

    MDR report key: 1942748 · Received December 10, 2010

    Report

    Report Number
    1831750-2010-04734
    Event Type
    Malfunction
    Date Received
    December 10, 2010
    Date of Event
    November 15, 2010
    Report Date
    November 15, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FPP
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULTS: ANKLE RESTRAINT STRAP.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT DURING PREVENTATIVE MAINTENANCE FOUND STAIR CHAIR MISSING RESTRAINT STRAP ANKLE. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1