BEUDAMED
    FDA Adverse Event Death Summary report: N

    ONETOUCH ULTRA STRIPS

    MDR report key: 14945723 · Received July 6, 2022

    Report

    Report Number
    MW5110704
    Event Type
    Death
    Date Received
    July 6, 2022
    Report Date
    July 1, 2022
    Manufacturer
    LIFESCAN, INC.
    Product Code
    NBW
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    NO INFORMATION
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    PATIENT DECEASED, WAS NOT ON MEDICATION AT THE TIME. FDA SAFETY REPORT ID# (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2087261 ONETOUCH ULTRA STRIPS SYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER NBW LIFESCAN, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 Female Death