BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STRYKER GO BED

    MDR report key: 2033187 · Received February 28, 2011

    Report

    Report Number
    1831750-2011-01952
    Event Type
    Malfunction
    Date Received
    February 28, 2011
    Date of Event
    December 13, 2010
    Report Date
    December 13, 2010
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NV, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT: DRIED GREASE ON LOCKING MECHANISM.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SIDERAILS COULD NOT BE LOCKED INTO POSITION. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRYKER GO BED A/C HOSPITAL BED FNL STRYKER MEDICAL 2500700000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1