BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED II

    MDR report key: 2861808 · Received November 8, 2012

    Report

    Report Number
    1831750-2012-11703
    Event Type
    Malfunction
    Date Received
    November 8, 2012
    Date of Event
    October 11, 2012
    Report Date
    October 12, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    CUSTOMER PERFORMED EVALUATION. LOAD CELL, STRYKER SERVICE REP TO DO REPAIRS.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE SCALE WAS NOT ACCURATE. THERE WAS NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED II A/C HOSPITAL BED FNL STRYKER MEDICAL FL28EX NA

    Patients

    Seq Age Sex Outcome Treatment
    1