BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DRIVE DELTA PRO BED FULL ELECTRIC

    MDR report key: 22717578 · Received August 5, 2025

    Report

    Report Number
    MW5174029
    Event Type
    Injury
    Date Received
    August 5, 2025
    Date of Event
    June 16, 2025
    Report Date
    July 26, 2025
    Manufacturer
    MEDICAL DEPOT, INC.
    Product Code
    FNL
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    VA, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    HEAD OF BED WAS ELEVATED. SUDDENLY AND WITHOUT WARNING IT COLLAPSED. WIFE STRUCK HEAD. INJURY NOT SEVERE BUT IF IT HAD STRUCK THE HEADBOARD HARDER, SHE COULD HAVE BEEN KNOCKED UNCONSCIOUS OR EVEN HAD A SEROUS SPINAL NECK INJURY. BED WAS "DRIVE DELTA PRO BEDFULL ELECTRIC" ITEM 491760037007. BED WAS REPAIRED BY SELLER. FEEL THE COLLAPSE COULD HAPPEN AGAIN. BED NOT SAFE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1568342 DRIVE DELTA PRO BED FULL ELECTRIC BED, AC-POWERED ADJUSTABLE HOSPITAL FNL MEDICAL DEPOT, INC. 491760037007

    Patients

    Seq Age Sex Outcome Treatment
    1 83 YR Female Required Intervention