BEUDAMED
    FDA Adverse Event Injury Summary report: N

    INX FOR INLINE

    MDR report key: 24756717 · Received April 1, 2026

    Report

    Report Number
    1523574-2026-00026
    Event Type
    Injury
    Date Received
    April 1, 2026
    Date of Event
    March 1, 2026
    Report Date
    April 16, 2026
    Manufacturer
    FERNO-WASHINGTON, INC.
    Product Code
    FPO
    UDI-DI
    00190790001339
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KS, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    THE SUBJECT STRETCHER WAS RETURNED TO MANUFACTURER FOR A VISUAL AND FUNCTIONAL EVALUATION. IT WAS CONFIRMED A MOUNTING BLOCK HAD BROKEN WHICH RESULTED IN THE UNINTENDED MOVEMENT OF THE LEG ASSEMBLY THE STRETCHER WAS REPAIRED AND RETURNED TO SERVICE.

    Description of Event or Problem · 0

    THE END USER REPORTED WHILE UNLOADING A PATIENT FROM THE AMBULANCE ON THE STRETCHER, AFTER THE LEGS WERE EXTENDED TO THE GROUND AND THE LOAD END OPERATOR RELEASED THE SAFETY BAIL, ONE OF THE STRETCHER LEGS "BROKE" RESULTING IN UNINTENDED MOVEMENT OF THE STRETCHER. THE PATIENT WAS NOT INJURED; HOWEVER, THE MEDIC'S ARM WAS PINNED BETWEEN THE STRETCHER AND THE BACK OF THE AMBULANCE. THE MEDIC SOUGHT MEDICAL EVALUATION AND THE RESULTING INJURY WAS A BRUISE AND THE MEDIC WAS RELEASED BACK TO WORK. AN EVALUATION OF THE STRETCHER HAS BEEN INITIATED.

    Description of Event or Problem · 0

    THE END USER REPORTED WHILE UNLOADING A PATIENT FROM THE AMBULANCE ON THE STRETCHER, AFTER THE LEGS WERE EXTENDED TO THE GROUND AND THE LOAD END OPERATOR RELEASED THE SAFETY BAIL, ONE OF THE STRETCHER LEGS "BROKE" RESULTING IN UNINTENDED MOVEMENT OF THE STRETCHER. THE PATIENT WAS NOT INJURED; HOWEVER, THE MEDIC'S ARM WAS PINNED BETWEEN THE STRETCHER AND THE BACK OF THE AMBULANCE. THE MEDIC SOUGHT MEDICAL EVALUATION AND THE RESULTING INJURY WAS A BRUISE AND THE MEDIC WAS RELEASED BACK TO WORK. AN EVALUATION OF THE STRETCHER HAS BEEN INITIATED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    470784 INX FOR INLINE INX FOR INLINE FPO FERNO-WASHINGTON, INC. 0015811 M991690 00190790001339

    Patients

    Seq Age Sex Outcome Treatment
    1