BEUDAMED
    FDA Adverse Event Death Summary report: N

    MEDI-MAN ELECTRIC LIFT

    MDR report key: 292027 · Received August 23, 2000

    Report

    Report Number
    MW4002832
    Event Type
    Death
    Date Received
    August 23, 2000
    Date of Event
    March 1, 2000
    Report Date
    August 23, 2000
    Manufacturer
    MEDI MAN REHABILITATION INC
    Product Code
    FNG
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THESE LIFTS HAVE HAD SEVERAL CATASTROPHIC FAILURES. DURING THE MOST RECENT FAILURE THE PT DIED. RPTR INDICATED THAT THE DEATH HAD BEEN REPORTED TO FDA, AND THE HEALTH DEPT HAD JUST HAD THE NURSING HOME, WHERE THE PT WAS KILLED, IN FOR A MEETING TO DISCUSS THE PROBLEM. RPTR INDICATED THAT THE FIRM DIDN'T SEEM TO CARE ABOUT THE PROBLEM WHEN THEY WERE CONTACTED BY THE NURSING HOME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MEDI-MAN ELECTRIC LIFT ELECTRIC LIFT FNG MEDI MAN REHABILITATION INC NI NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO Death