BEUDAMED
    FDA Adverse Event Injury Summary report: N

    93 ES SQUADMATE

    MDR report key: 17413812 · Received July 28, 2023

    Report

    Report Number
    1523574-2023-00028
    Event Type
    Injury
    Date Received
    July 28, 2023
    Date of Event
    July 21, 2023
    Report Date
    January 4, 2024
    Manufacturer
    FERNO-WASHINGTON, INC.
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    A VISUAL AND FUNCTIONAL EVALUATION OF THE SUBJECT STRETCHER WAS CONDUCTED BY AN AUTHORIZED FIELD TECHNICIAN AT THE CUSTOMER'S LOCATION. THE STRETCHER WAS FOUND TO BE OPERATING AS INTENDED AND THE ALLEGED ISSUE COULD NOT BE DUPLICATED. NO REPAIRS WERE MADE AND THE STRETCHER WAS RETURNED TO SERVICE.

    Description of Event or Problem · 0

    AFTER UNLOADING THE PATIENT FROM THE AMBULANCE THE LEGS OF THE STRETCHER ALLEGEDLY DID NOT LOCK AND THE STRETCHER LOWERED TO THE BOTTOM POSITION. THE PATIENT REMAINED RESTRAINED TO THE STRETCHER AND IT WAS NOT REPORTED THAT THE STRETCHER TIPPED. ALLEGED INJURY TO THE PATIENT AND MEDIC WERE DESCRIBED AS GENERAL PAIN TO BACK AND ARM. MEDICAL INTERVENTION SOUGHT WAS EVALUATION ONLY. NO OTHER DETAILS ON THE ALLEGED INJURY WERE PROVIDED.

    Description of Event or Problem · 0

    AFTER UNLOADING THE PATIENT FROM THE AMBULANCE THE LEGS OF THE STRETCHER ALLEGEDLY DID NOT LOCK AND THE STRETCHER LOWERED TO THE BOTTOM POSITION. THE PATIENT REMAINED RESTRAINED TO THE STRETCHER AND IT WAS NOT REPORTED THAT THE STRETCHER TIPPED. ALLEGED INJURY TO THE PATIENT AND MEDIC WERE DESCRIBED AS GENERAL PAIN TO BACK AND ARM. MEDICAL INTERVENTION SOUGHT WAS EVALUATION ONLY. NO OTHER DETAILS ON THE ALLEGED INJURY WERE PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2326689 93 ES SQUADMATE 93 ES SQUADMATE FPO FERNO-WASHINGTON, INC. 0015574

    Patients

    Seq Age Sex Outcome Treatment
    1 Male Other