BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GO BED PLUS

    MDR report key: 2142784 · Received June 20, 2011

    Report

    Report Number
    1831750-2011-06193
    Event Type
    Malfunction
    Date Received
    June 20, 2011
    Date of Event
    May 23, 2011
    Report Date
    May 23, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    HEAVY CORROSION AND WEAR INSIDE PIVOT POINT WHERE SIDERAIL ARMS ATTACH TO SIDERAIL.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD LEFT SIDE RAIL WOULD NOT RAISE, LOWER OR LOCK IN THE UPRIGHT POSITION. IT IS UNKNOWN IF THERE WAS PATIENT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GO BED PLUS A/C HOSPITAL BED FNL STRYKER MEDICAL 2501 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK