Thor Photomedicine recalls
Thor Photomedicine has 9 recalls on record with the FDA and USDA, the earliest in 2023 and the latest reported on 3 Sep 2025. 9 are still ongoing. The most frequent reason is device malfunction.
Total recalls9since 2023
Last 12 months0reported
Class I00% of total
Ongoing9latest 3 Sep 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 9 100%Class III 0 0%
Why thor photomedicine is recalled
Product types
By year
Ongoing thor photomedicine recalls
9 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Brand Name: Thor Product Name: NovoTHOR Model/Catalog Number: S2188 recalled | Thor Photomedicine | Temperature Abuse | Nationwide |
| Device | CLASS II | NovoTHOR Gen 3.0 Reg PRX recalled by THOR Photomedicine | Thor Photomedicine | Temperature Abuse | Nationwide |
| Device | CLASS II | NovoTHOR XL recalled by THOR Photomedicine | Thor Photomedicine | Temperature Abuse | Nationwide |
| Device | CLASS II | NovoTHOR Gen 3.0 Reg PRX recalled by THOR Photomedicine | Thor Photomedicine | Temperature Abuse | Nationwide |
| Device | CLASS II | NovoTHOR Whole Body Light Pod, Gen 3.0 Product recalled | Thor Photomedicine | Other | 17 states |
| Device | CLASS II | NovoTHOR Gen whole body red light therapy bed recalled | Thor Photomedicine | Device Malfunction | Nationwide |
All thor photomedicine recalls, newest first
9 totalAbout this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.