Medical Device Recall: Z-0003-2023

FDA Recalls dataset · Firm: IN MY BATHROOM LLC · Status: Open, Classified

Recall Action Class: N/A Date Initiated: 2022-01-27 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0003-2023.

Recall Res Number
Z-0003-2023
Recalling Firm / Manufacturer
IN MY BATHROOM LLC
FEI Number
3016850352
Recall Status
Open, Classified
Recall Classification
N/A
Date Initiated
2022-01-27
Date Posted
2022-10-05
Date Terminated
N/A
Product Code
RHP
Event Number
90860
Product Quantity
485 units
Product 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 for Recall Excessive ultraviolet-C radiation
Action Details 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 Pattern US Nationwide Distribution
Code Information / Serial Numbers Model Seago SG-153

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