BEUDAMED
    FDA Adverse Event Summary report: N

    CVS BRAND MANUAL BLOOD PRESSURE CUFF

    MDR report key: 7925922 · Received October 1, 2018

    Report

    Report Number
    MW5080246
    Date Received
    October 1, 2018
    Date of Event
    September 8, 2018
    Report Date
    September 9, 2018
    Manufacturer
    CVS PHARMACY INC.
    Product Code
    DXN
    Report Source
    Voluntary report
    Reporter Location
    MD, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I PURCHASED A MANUAL BLOOD PRESSURE CUFF FROM (B)(6) IN (B)(6). I TOOK THE BP OF A FRIEND, WHOSE TYPICAL BLOOD PRESSURE IS 130/75, AND MY OWN, WHICH IS TYPICALLY 110/60. THE PRESSURE GAUGE READ 140/100 FOR BOTH READINGS. I AM A NURSE, IN PRACTICE FOR OVER 25 YEARS, AND VERY FAMILIAR WITH MANUAL BLOOD PRESSURE PRACTICE. I RETURNED THE PRODUCT TO (B)(6) THE NEXT DAY AND REPORTED THE PROBLEM TO THEM AND SUGGESTED THAT THEY HAVE THEIR (B)(6) NURSE PRACTITIONERS TRIAL THIS PRODUCT. DOCUMENT NUMBER: (B)(4). REPORT NUMBER: (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    765079 CVS BRAND MANUAL BLOOD PRESSURE CUFF SYSTEM MEASUREMENT BLOOD PRESSURE - NONINVASIVE DXN CVS PHARMACY INC.

    Patients

    Seq Age Sex Outcome Treatment
    1