BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECA 703

    MDR report key: 9699166 · Received February 12, 2020

    Report

    Report Number
    9699166
    Event Type
    Malfunction
    Date Received
    February 12, 2020
    Date of Event
    February 10, 2020
    Report Date
    February 10, 2020
    Manufacturer
    SECA CORP.
    Product Code
    FRI
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    FL
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    THE POWER SUPPLY CORD OF THE SECA SCALES BEING USE ON SECA SCALES MODEL 703 AND 727 ARE STARTING TO KNOT, TWIST, AND BREAK. ALL THESE SYMPTOMS ARE STARTING TO CAUSE SECA POWER SUPPLY CORDS TO FAIL AT HIGHER RATES AND COULD DEVELOP INTO SAFETY ISSUES FOR USERS AND/OR PATIENTS. MANUFACTURER RESPONSE FOR SCALE, STAND-ON, PATIENT, SECA 703 (PER SITE REPORTER). MANUFACTURER HAS BEEN CONTACTED IN REGARDS TO THE POWER CORD DESIGN AND ITS FRAGILE CONSTRUCTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    161479 SECA 703 SCALE, STAND-ON, PATIENT FRI SECA CORP. 703

    Patients

    Seq Age Sex Outcome Treatment
    1 0 DA