BEUDAMED
    FDA Adverse Event Death Summary report: N

    STRYKER OB/GYN STRETCHER

    MDR report key: 272677 · Received April 6, 2000

    Report

    Report Number
    1831750-2000-00003
    Event Type
    Death
    Date Received
    April 6, 2000
    Date of Event
    March 16, 2000
    Report Date
    April 6, 2000
    Manufacturer
    STRYKER CORPORATION MEDICAL DIVISION
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    A PT ALLEGEDLY RELEASED THE SIDERAIL LATCH ON THEIR OWN, LOWERED THE SIDERAIL, AND EXITED THE STRETCHER. ALLEGEDLY THE PT SUBSEQUENTLY FELL AND EXPIRED FROM CIRCUMSTANCES RELATED TO THE FALL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRYKER OB/GYN STRETCHER HOSPITAL STRETCHER FPO STRYKER CORPORATION MEDICAL DIVISION 1060 *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Death