BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STRYKER GO BED

    MDR report key: 2904445 · Received November 30, 2012

    Report

    Report Number
    1831750-2012-12443
    Event Type
    Malfunction
    Date Received
    November 30, 2012
    Date of Event
    November 2, 2012
    Report Date
    November 2, 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

    (B)(4): RUST/CORROSION.

    Description of Event or Problem · 1

    THE CUSTOMER ALLEGED THE SIDERAILS WERE STUCK DOWN AND UNABLE TO LATCH IN THE UPRIGHT POSITION. NO PT INVOLVEMENT OR ADVERSE EVENTS 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