BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MA204

    MDR report key: 2112522 · Received May 25, 2011

    Report

    Report Number
    1831750-2011-05049
    Event Type
    Malfunction
    Date Received
    May 25, 2011
    Date of Event
    April 27, 2011
    Report Date
    April 27, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MD, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    LIFT MOTORS SET INCORRECTLY.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SCALE WAS NOT WEIGHING ACCURATELY. THERE WAS PT INVOLVEMENT; HOWEVER NO ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MA204 A/C HOSPITAL BED FNL STRYKER MEDICAL FL25E NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK