BEUDAMED
    FDA Adverse Event Injury Summary report: N

    STRYKER ICU BED

    MDR report key: 222170 · Received May 5, 1999

    Report

    Report Number
    1831750-1999-00005
    Event Type
    Injury
    Date Received
    May 5, 1999
    Report Date
    April 28, 1999
    Manufacturer
    STRYKER CORP MEDICAL DIV
    Product Code
    FNL
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    A HOSP STAFF MEMBER ALLEGEDLY FRACTURED AN ANKLE WHILE RELEASING THE BRAKES ON A MODEL 2020 CRITICAL CARE BED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRYKER ICU BED ICU BED FNL STRYKER CORP MEDICAL DIV 2020 *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Required Intervention