BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED II

    MDR report key: 2160720 · Received June 30, 2011

    Report

    Report Number
    1831750-2011-06657
    Event Type
    Malfunction
    Date Received
    June 30, 2011
    Date of Event
    June 1, 2011
    Report Date
    June 2, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    BENT FOWLER MOTOR TUBE.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE FOWLER TUBE WAS BENT. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED II A/C HOSPITAL BED FNL STRYKER MEDICAL FL28EX NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK