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THOR Photomedicine Ltd FDA Recalls

9 recalls on file across devices, 0 of them Class I and 9 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product
Brand Name: THOR Product Name: NovoTHOR XL Model/Catalog Number: S2190 Software Version: N/A Product Description: ThClass IIJul 24, 2025The potential for a failed welded nut to shear off. When thi
Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software Version: N/A Product Description: The NClass IIJul 24, 2025The potential for a failed welded nut to shear off. When thi
Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2186 Software Version: N/A Product DeClass IIJul 24, 2025The potential for a failed welded nut to shear off. When thi
Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2189 Software Version: N/A Product DeClass IIJul 24, 2025The potential for a failed welded nut to shear off. When thi
NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 - Reg PRX (3) Product CoClass IINov 20, 2023One of the ball studs attaching a gas strut to the canopy ma
NovoTHOR Gen 2.5 XL whole body red light therapy bed, model S2184.Class IISep 13, 2022Failure of ball stud components causing the gas strut on one
NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176Class IISep 13, 2022Failure of ball stud components causing the gas strut on one
NovoTHOR Gen 2.5 Regular whole body red light therapy bed, model S2183Class IISep 13, 2022Failure of ball stud components causing the gas strut on one
G041 POD, THOR NOVO GEN 2.0 XL whole body red light therapy bed, model S1177Class IISep 13, 2022Failure of ball stud components causing the gas strut on one

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