LightStrike Blackout Curtains — Class II medical device recall Z-1615-2024
Ongoing recall by XENEX Disinfection Services Inc., reported 2024-05-01, distributed nationwide. Blackout curtains are no longer recommended as a protective barrier against UV/Ozone exposure to a bystander s
| Recall number | Z-1615-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | XENEX Disinfection Services Inc., San Antonio, TX, United States |
| Recall initiated | 2024-03-18 |
| Classified | 2024-04-23 |
| Reported by FDA | 2024-05-01 |
| Distributed | Nationwide (US) |
| Quantity | 377 |
| Reason classes | microbial contamination |
| UPC / GTIN / UDI-DI | 00814122020033, 00814122020064, 00814122020125, 00814122020132 |
| Model numbers | 610-00008, 610-00009, 610-00019, 610-00020, 610-00024, LSMUV6-FT, LSMUV6-SL, PXUV4D, PXUV5D |
Product
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.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1615-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.