BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TREATMENT RECLINER

    MDR report key: 1870457 · Received October 6, 2010

    Report

    Report Number
    1831750-2010-02703
    Event Type
    Malfunction
    Date Received
    October 6, 2010
    Date of Event
    September 1, 2010
    Report Date
    September 1, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIVISON
    Product Code
    FRK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    INVESTIGATION UNDERWAY.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE RECLINER BACK SECTION WILL NOT PROPERLY ATTACH TO THE SEAT SECTION. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TREATMENT RECLINER EXAMINATION AND TREATMENT CHAIR FRK STRYKER CORP, MEDICAL DIVISON 3500000710 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA