Reported Sep 3, 2025 · Ongoing
Brand Name: THOR Product Name: NovoTHOR Gen 3.0 Reg PRX Model/Catalog Number: S2186 Software Version: N/A Product…
THOR Photomedicine Ltd.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: THOR Photomedicine Ltd · 2 Anglo Office Park · Amersham · N/A
Is this the product you have?
- Brand NameTHOR
- Product NameNovoTHOR Gen 3.0
- Reg PRX Model/Catalog NumberS2186
- Software VersionN/A
- Product DescriptionThe 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 for temporary increase in local blood circulation, temporary relief of minor muscle and joint pain and stiffness, minor arthritis pain, muscle spasm, and temporary relaxation of muscles
- ComponentN/A
- Lot codes and dates
- Model/Catalog NumberS2186
- UDI-DISerial
- numbers
40054062
- Amount recalled
- 2 units (1 US, 1 OUS)
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was recalled
The potential for a failed welded nut to shear off. When this occurs, the gas strut on one side of the device becomes detached from the canopy, making the canopy difficult to lift.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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