BEUDAMED
    FDA Adverse Event Other Summary report: N

    REMANUFACTURED BED

    MDR report key: 1378329 · Received April 30, 2009

    Report

    Report Number
    1824206-2009-02084
    Event Type
    Other
    Date Received
    April 30, 2009
    Date of Event
    April 3, 2009
    Report Date
    April 3, 2009
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN INVESTIGATED AND FOUND NO PROBLEMS WITH THE BED. THE BED DID NOT HAVE HBSW KITS OR Z-INSERTS INSTALLED.

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATES THE PATIENT BECAME ENTRAPPED IN ZONE 1.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 REMANUFACTURED BED AC POWERED HOSPITAL BED FNL HILL-ROM RITTER 8350

    Patients

    Seq Age Sex Outcome Treatment
    1 47 YR