BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GO BED PLUS

    MDR report key: 2914919 · Received December 7, 2012

    Report

    Report Number
    1831750-2012-12662
    Event Type
    Malfunction
    Date Received
    December 7, 2012
    Date of Event
    November 26, 2012
    Report Date
    November 26, 2012
    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

    RESULT: CORROSION.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE LEFT HEAD SIDERAIL WOULD NOT LOCK IN THE UPRIGHT POSITION. NO PT INVOLVEMENT OR 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