BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    KENDALL SCD 700 SERIES

    MDR report key: 14407072 · Received May 16, 2022

    Report

    Report Number
    14407072
    Event Type
    Malfunction
    Date Received
    May 16, 2022
    Date of Event
    April 29, 2022
    Report Date
    May 3, 2022
    Manufacturer
    COVIDIEN LLC
    Product Code
    JOW
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MA
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    SCD (SEQUENTIAL COMPRESSION DEVICE) BOOT MACHINE ONLY SENSING FOOT SLEEVES. COMPRESSION SLEEVES EXCHANGE BUT STILL ONLY SENSING BILATERAL FOOT SLEEVES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2030750 KENDALL SCD 700 SERIES SLEEVE, LIMB, COMPRESSIBLE JOW COVIDIEN LLC

    Patients

    Seq Age Sex Outcome Treatment
    1 24090 DA Female