BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LIFE SAFETY PRODUCTS (LSP)

    MDR report key: 8854596 · Received August 2, 2019

    Report

    Report Number
    MW5088635
    Event Type
    Injury
    Date Received
    August 2, 2019
    Date of Event
    July 21, 2019
    Report Date
    August 1, 2019
    Manufacturer
    ALLIED HEALTHCARE PRODUCTS, INC.
    Product Code
    CAN
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CT, US
    Reporter Occupation
    EMERGENCY MEDICAL TECHNICIAN

    Narratives

    Description of Event or Problem · 1

    CALLER CALLED TO REPORT THAT ON (B)(6) 2019 IN THE EVENING EMERGENCY MEDICAL SERVICES WAS CALLED TO TRANSPORT A PT TO (B)(6); ON ARRIVAL INTO THE HOSP WITH THE PT ON THE STRETCHER CONNECTED TO OXYGEN BOTTLE, THE EMT NOTICED THAT THE REGULATOR THAT WAS ATTACHED TO THE STRETCHER WAS NOT IN THE ON POSITION. ONCE HE TURNED THE REGULATOR ON, THE DEVICE COMBUSTED INTO FLAMES. THE EMT SUFFERED SECOND DEGREE BURNS TO HIS HAND AND THE PT ON THE STRETCHER HAD MINOR BURNS TO THE TOP HEAD AND HIS HAIR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    649814 LIFE SAFETY PRODUCTS (LSP) REGULATOR, PRESSURE, GAS CYLINDER CAN ALLIED HEALTHCARE PRODUCTS, INC. 270-20

    Patients

    Seq Age Sex Outcome Treatment
    1 Life Threatening| O| S