BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STAIR PRO - MODEL 6252

    MDR report key: 2221841 · Received July 21, 2011

    Report

    Report Number
    1831750-2011-07455
    Event Type
    Malfunction
    Date Received
    July 21, 2011
    Date of Event
    June 23, 2011
    Report Date
    June 23, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPP
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    OTHER - BUCKLE ON RESTRAINT STRAP.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BUCKLE ON THE RESTRAINT STRAP WAS BROKEN. 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 MEDICAL 6252 NA

    Patients

    Seq Age Sex Outcome Treatment
    1