Cavitron® 8270310Recalls & reported problems
Dentsply Professional · Cavitron® 300 Series, 115V Domestic Ultrasonic Scaler · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI D00382703101), received between Dec 16, 2025 and Apr 3, 2026 — classified as 8 malfunctions.
The most frequently reported specific device problem is “Overheating of Device” (5 reports).
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.
Reports received per month
Most reported problems
Device problems
- Overheating of Device5
- No Flow2
- Restricted Flow rate1
Patient problems
- No Clinical Signs, Symptoms or Conditions8
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 3, 2026Overheating of Device
WHILE THE CUSTOMER WAS USING A CAVITRON 300 SERIES G310, THEY ALLEGE THAT THE INSERT IS GETTING HOT. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24775099 ↗MalfunctionMar 4, 2026No Flow
WHILE USING A CAVITRON 300 SERIES G310 THEY ALLEGE THAT THEY HAVE NO WATER FLOW AND THE HANDPIECE IS HEATING UP,; NO INJURY RESULTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24512678 ↗MalfunctionFeb 24, 2026No Flow
WHILE USING A CAVITRON 300 SERIES G310, THEY ALLEGE THAT THEY HAVE NO WATER AND THE UNIT IS GETTING WARM, NO INJURY RESULTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24428790 ↗MalfunctionJan 13, 2026Overheating of Device
WHILE THE CUSTOMER WAS USING A CAVITRON 300 SERIES G310, THEY ALLEGE THAT THE STERIMATE AND INSERTS ARE GETTING VERY HOT, NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24056742 ↗MalfunctionJan 5, 2026Overheating of Device
WHILE THE CUSTOMER WAS USING A CAVITRON 300 SERIES G310, THEY ALLEGE THAT THE INSERTS ARE HEATING UP. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23967306 ↗MalfunctionDec 28, 2025Overheating of Device; Overheating of Device
WHILE THE CUSTOMER WAS USING A CAVITRON 300 SERIES G310 THEY ALLEGE THAT THE INSERT HEATS UP. NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23903718 ↗MalfunctionDec 16, 2025Overheating of Device; Overheating of Device
WHILE THE CUSTOMER WAS USING A CAVITRON 300 SERIES G310, THEY ALLEGE THAT THE HANDPIECE AND INSERT ARE GETTING HOT, NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23817576 ↗MalfunctionDec 16, 2025Restricted Flow rate; Restricted Flow rate
WHILE USING A CAVITRON 300 SERIES G310 THEY ALLEGE THAT THEY HAVE INCONSISTENT WATER FLOW AND THE HANDPIECE IS GETTING HOT, NO INJURY RESULTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23817574 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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