BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FL14E1

    MDR report key: 2172325 · Received December 9, 2010

    Report

    Report Number
    1831750-2010-04696
    Event Type
    Malfunction
    Date Received
    December 9, 2010
    Date of Event
    November 11, 2010
    Report Date
    November 11, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    FOOTBOARD.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT BOARD IS DAMAGED BEYOND REPAIR. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FL14E1 AC POWERED HOSPITAL BED FNL STRYKER CORP., MEDICAL DIV. FL14E1 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK