BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ELECTRIC MED/SURG BED

    MDR report key: 2161906 · Received May 20, 2011

    Report

    Report Number
    9680128-2011-05154
    Event Type
    Malfunction
    Date Received
    May 20, 2011
    Date of Event
    April 29, 2011
    Report Date
    April 29, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    DAMAGED ACTUATOR ROD.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOWLER WILL NOT GO DOWN. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ELECTRIC MED/SURG BED A/C HOSPITAL BED FNL STRYKER MEDICAL FL23E NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK