BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NURSE ASSIST, INC

    MDR report key: 829377 · Received August 9, 2005

    Report

    Report Number
    1650927-2005-00005
    Event Type
    Malfunction
    Date Received
    August 9, 2005
    Date of Event
    June 1, 2005
    Report Date
    August 9, 2005
    Product Code
    KMI
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    THE LOT OF POWER SUPPLIES USED EXCLUSIVELY FOR THIS FACILITY APPEARS TO HAVE SOME UNIQUE WEAKNESS WITH THE AC BLADE RETENTION. REPLACEMENT SUPPLIES HAVE BEEN SENT TO THE FACILITY AND FURTHER DESIGN ENHANCEMENTS HAVE BEEN INITIATED TO BOLSTER THE RUGGED-NESS OF THE POWER SUPPLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NURSE ASSIST, INC KMI NA

    Patients

    Seq Age Sex Outcome Treatment
    1 Other