Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LightStrike Blackout Curtains Recalled by XENEX Disinfection Services Inc. Due to Blackout curtains are no longer recommended as a...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact XENEX Disinfection Services Inc. directly.
Affected Products
LightStrike Blackout Curtains, Part numbers; 610-00008, 610-00009, 610-00019, 610-00020, and 610-00024, used with the LightStrike Germ-Zapping Robots Models: PXUV4D, PXUV5D, LSMUV6-FT, or LSMUV6-SL, for whole room microbial reduction.
Quantity: 377
Why Was This Recalled?
Blackout curtains are no longer recommended as a protective barrier against UV/Ozone exposure to a bystander standing in the same room, but on the other side of the curtain from where a microbial reduction device UV cycle is taking place. Bystanders in the room during the cycle may experience temporary skin reddening, feeling of sand in eyes, nausea, headache, and/or mucous membrane irritation.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About XENEX Disinfection Services Inc.
XENEX Disinfection Services Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report