BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED II MED/SURG BED

    MDR report key: 1984607 · Received January 19, 2011

    Report

    Report Number
    1831750-2011-00665
    Event Type
    Malfunction
    Date Received
    January 19, 2011
    Date of Event
    December 22, 2010
    Report Date
    December 22, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    POWER INLET.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT ALLEGEDLY,THERE WAS NO POWER ON BED. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED II MED/SURG BED A/C HOSPITAL BED FNL STRYKER CORP., MEDICAL DIV. FL28C NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK