BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PATIENT ROOM ROCKER RECLINER

    MDR report key: 2873518 · Received November 15, 2012

    Report

    Report Number
    1831750-2012-11981
    Event Type
    Malfunction
    Date Received
    November 15, 2012
    Date of Event
    October 25, 2012
    Report Date
    October 25, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FRJ
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULTS - RECLINER MECHANISM.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT REST WOULD NOT LATCH CLOSED DUE TO THE RECLINING MECHANISM BEING BENT. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PATIENT ROOM ROCKER RECLINER RECLINER FRJ STRYKER MEDICAL 350000750 NA

    Patients

    Seq Age Sex Outcome Treatment
    1