Manufacturer

THOR Photomedicine Ltd

9 recalls in our database name THOR Photomedicine Ltd as the manufacturing or recalling firm.

What the numbers show

Total: 9
Critical: 0
Severe: 0
Most recent: 2025-09-03

Of the 9 recalls from THOR Photomedicine Ltd we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–9 of 9

ModerateFDA (Devices)·Z-2418-2025·2025-09-03
NovoTHOR Gen 3.0 unit recalled because gas strut may detach from canopy
A single NovoTHOR Gen 3.0 Reg PRX unit, model S2189, is recalled because a failed welded nut may shear off, detaching a gas strut from the canopy and making the canopy difficult to lift.
Product
Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2189 Software Version: N/A Product Description: The NovoTHOR and NovoTHOR XL are intended to emit energy in the visible and IR spectrum to provide topical heating for the purpose of elevating tissu
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2416-2025·2025-09-03
NovoTHOR light therapy devices recalled over welded nut that may shear
NovoTHOR devices, model S2188, are recalled because a failed welded nut may shear off, detaching a gas strut from the canopy and making the canopy difficult to lift. 80 units are affected.
Product
Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software Version: N/A Product Description: The NovoTHOR and NovoTHOR XL are intended to emit energy in the visible and IR spectrum to provide topical heating for the purpose of elevating tissue temperature fo
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2417-2025·2025-09-03
NovoTHOR XL devices recalled over failed welded nut detaching gas strut
NovoTHOR XL devices, model S2190, are recalled because a failed welded nut may shear off, detaching a gas strut from the canopy and making the canopy difficult to lift. 55 units are affected.
Product
Brand Name: THOR Product Name: NovoTHOR XL Model/Catalog Number: S2190 Software Version: N/A Product Description: The NovoTHOR and NovoTHOR XL are intended to emit energy in the visible and IR spectrum to provide topical heating for the purpose of elevating tissue temperature
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2419-2025·2025-09-03
Light therapy devices recalled over welded nut that may shear off
Two NovoTHOR Gen 3.0 Reg PRX units are recalled because a failed welded nut may shear off, detaching a gas strut from the canopy and making the canopy difficult to lift.
Product
Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2186 Software Version: N/A Product Description: The NovoTHOR and NovoTHOR XL are intended to emit energy in the visible and IR spectrum to provide topical heating for the purpose of elevating tissu
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0972-2024·2024-02-07
NovoTHOR Whole Body Light Pod Gen 3.0 Canopy Strut Ball Stud May Fail
A ball stud on the gas strut may fail on NovoTHOR Whole Body Light Pod units, potentially causing injury if the canopy malfunctions while someone is using the device.
Product
NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 - Reg PRX (3) Product Code S2190 - XL
Category
Medical Device
Distribution
17 states
HighFDA (Devices)·Z-0455-2024·2023-12-13
NovoTHOR Gen 2.5 Therapy Bed Recalled for Ball Stud Failure
Thor Photomedicine's NovoTHOR Gen 2.5 therapy beds are being recalled due to failure of ball stud components in the gas strut, which can detach from the canopy. This affects 26 units distributed across the US and internationally.
Product
NovoTHOR Gen 2.5 Regular whole body red light therapy bed, model S2183
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0454-2024·2023-12-13
Red Light Therapy Bed Canopy Strut Detachment Risk Nationwide
Thor Photomedicine is recalling six THOR NOVO GEN 2.0 XL whole body red light therapy beds due to ball stud component failure. The defect causes gas strut detachment, making the canopy difficult to lift.
Product
G041 POD, THOR NOVO GEN 2.0 XL whole body red light therapy bed, model S1177
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0453-2024·2023-12-13
NovoTHOR Gen 2.0 Light Therapy Bed Canopy Detachment Due to Ball Stud Failure
Thor Photomedicine is recalling 19 NovoTHOR Gen 2.0 red light therapy beds due to ball stud component failures that can cause canopy detachment or difficulty in lifting. The beds were distributed worldwide.
Product
NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0456-2024·2023-12-13
NovoTHOR Gen 2.5 XL Red Light Therapy Bed Canopy Gas Strut Detachment Recall
Thor Photomedicine is recalling 26 NovoTHOR Gen 2.5 XL red light therapy beds due to ball stud component failure that can cause the gas strut to detach, making the canopy difficult to lift.
Product
NovoTHOR Gen 2.5 XL whole body red light therapy bed, model S2184.
Category
Medical Device
Distribution
Distributed nationwide