BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED+

    MDR report key: 2232991 · Received July 25, 2011

    Report

    Report Number
    1831750-2011-07570
    Event Type
    Malfunction
    Date Received
    July 25, 2011
    Date of Event
    June 27, 2011
    Report Date
    June 27, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    GREASE DRIED ON SIDERAIL CAUSING IT NOT TO FUNCTION PROPERLY.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THE HEAD SIDERAIL WOULD NOT LOCK IN THE UP POSITION. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED+ A/C HOSPITAL BED FNL STRYKER MEDICAL FL20E NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK