Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2419-2025 — 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 tissue temperature for te

U.S. FDA — Device Enforcement · United Kingdom · 2025-07-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2419-2025
Date of alert
2025-07-24
Country / jurisdiction
United Kingdom
Risk level
Class II
Risk type
recall
Brand
THOR Photomedicine Ltd
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.