660nm 75mW Dental Probe 2.3Recalls & reported problems
Thor Photomedicine Limited · S2173 660nm 75mW Dental Probe · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05060494130114), received between Nov 27, 2024 and Nov 27, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
- Physical Resistance/Sticking1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 27, 2024Break; Physical Resistance/Sticking; Break; Physical Resistance/Sticking
NO ADVERSE EVENT OR USER HARM REPORTED. THIS MDR IS BEING SUBMITTED AS A VERBAL REPORT ON 16 SEPT 2024 NOTED THE "LIGHT GUIDE BROKE OFF INTO THE HAND OF A NURSE WHO WAS TRYING TO UN-JAM IT"; NO USER HARM OCCURRED, THE USER DID NOT MENTION ANY CONCERN OF POSSIBLE HARM AT ANY POINT. THIS VERBAL REPORT RELATES TO AN EARLIER REPAIR REQUEST ON JUNE 23 2024 STATING "THE USERS GOT ROUGH WITH HANDPIECE WHILE REMOVING THE BLACK PLASTIC TIP. THE TIP LENSES WERE BROKEN AND NOW A NEW TIP WILL NOT INSERT IN THE HANDPIECE. THEY MUST HAVE BENT THE INTERNAL AREA THAT THE TIP FITS INTO".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20794891 ↗
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
- NovoTHOR Gen 3.0 Reg PRXThor Photomedicine Limited · Lamp, Infrared, Therapeutic Heating1 recall0 reports
- 810nm 1W Cluster (5x200mW) 2.0Thor Photomedicine Limited · Lamp, Infrared, Therapeutic Heating3 reports
- CHATTANOOGA 27812Djo, LLC · Lamp, infrared, therapeutic heating3 reports
- CHATTANOOGA 27840Djo, LLC · Lamp, infrared, therapeutic heating2 reports
- LightForce FXi LTC-1500Litecure LLC · Lamp, Infrared, Therapeutic Heating1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page