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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.

FDA Recall Z-0003-2023 · Posted 2022-10-05

Recalling FirmIN MY BATHROOM LLC
Recall StatusOpen, Classified
Product CodeRHP
Date Initiated2022-01-27
Product Quantity485 units

Reason for Recall

Excessive ultraviolet-C radiation

Firm 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).

Root Cause

Radiation Control for Health and Safety Act

Distribution Pattern

US Nationwide Distribution

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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