[Recalled] 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
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| 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 for temporary increase |
|---|---|
| Brand / manufacturer | THOR Photomedicine Ltd |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2416-2025 |
| Country of notice | United Kingdom |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 24 July 2025 |
| EAN / barcode | 05060494130503 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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 Class II recall concerns device products distributed in United Kingdom and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from THOR Photomedicine Ltd
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.