FDAMarch 18, 2024device

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

xenex disinfection servicesxenexxenex disinfection

UPCs

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Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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