BEUDAMED
    FDA Adverse Event Death Summary report: N

    *

    MDR report key: 239433 · Received September 8, 1999

    Report

    Report Number
    1824206-1999-00012
    Event Type
    Death
    Date Received
    September 8, 1999
    Date of Event
    August 21, 1999
    Manufacturer
    HBR
    Product Code
    FNL
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    INFO RECEIVED FROM ADMINISTRATOR OF THE FACILITY INDICATED THAT A PT WAS FOUND DECEASED WITH HEAD IN SIDERAIL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * ELECTRIC BED FNL HBR 70 *

    Patients

    Seq Age Sex Outcome Treatment
    1 101 YR Death