BEUDAMED
    FDA Recall Open, Classified

    The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.

    Recall: Z-0003-2023 · Initiated January 27, 2022

    Recall

    Recall Number
    Z-0003-2023
    Event Number
    90860
    Firm
    IN MY BATHROOM LLC
    FEI Number
    3016850352
    Product Code
    RHP
    Status
    Open, Classified
    Root Cause
    Radiation Control for Health and Safety Act
    Initiated
    January 27, 2022
    Posted
    October 5, 2022
    Address
    22617 Mariano St, Woodland Hills, CA, 91367-6127

    Description

    The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.

    Reason

    Excessive ultraviolet-C radiation

    Action

    The firm issued and Urgent Electronic Device Recall letter dated September 9, 2022. Please complete and return the Electronic Device Recall Return Response form below as soon as possible to acknowledge receipt of this letter and initiate the process of sending back your UVILIZER Flip (Model Seago SG-153).

    Distribution

    US Nationwide Distribution

    Quantity

    485 units