NovoTHOR Gen 3.0 Reg PRXRecalls & reported problems
Thor Photomedicine Limited · S2189 NovoTHOR Gen 3.0 Reg PRX · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Jul 24, 2025Open, Classified
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.
Z-2418-2025 · Root cause: Process control · FDA record ↗
Other Lamp, Infrared, Therapeutic Heating devices
- NovoTHOR 3.0Thor Photomedicine Limited · Lamp, Infrared, Therapeutic Heating2 recalls0 reports
- NovoTHOR XL 3.0Thor Photomedicine Limited · Lamp, Infrared, Therapeutic Heating2 recalls0 reports
- NovoTHOR PRX 3.0Thor Photomedicine Limited · Lamp, Infrared, Therapeutic Heating1 recall0 reports
- CHATTANOOGA 27812Djo, LLC · Lamp, infrared, therapeutic heating3 reports
- 810nm 1W Cluster (5x200mW) 2.0Thor Photomedicine Limited · Lamp, Infrared, Therapeutic Heating3 reports
- CHATTANOOGA 27840Djo, LLC · Lamp, infrared, therapeutic heating2 reports
- 810nm 16W Cluster PRX100 (80x200mW) 2.3Thor Photomedicine Limited · Lamp, Infrared, Therapeutic Heating1 report
- CHATTANOOGA 27816Djo, LLC · Lamp, infrared, therapeutic heating1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.