Enhance® Finishing System 624065Recalls & reported problems
Dentsply International Inc. · Enhance® Finishing System POINT Refill Package, 40 Points · Class 1
- 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 D0026240651), received between Jun 18, 2026 and Jun 18, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 18, 2026Detachment of Device or Device Component
IN THIS EVENT IT IS REPORTED THAT FINISHING POINT RA REFILL IS ALLEGED TO HAVE A LATCHING ISSUE. THE OUTCOME OF THIS EVENT IS UNKNOWN AS OF THIS MDR. FURTHER INFORMATION REQUESTED.
Patient problems: Insufficient Information
MAUDE report 25545712 ↗
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- Nupro® Prophy Paste with Fluoride 801120Dentsply International Inc. · AGENT, POLISHING, ABRASIVE, ORAL CAVITY1 report
- NUPRO® Prophylaxis Paste with Fluoride 801232Dentsply International Inc. · AGENT, POLISHING, ABRASIVE, ORAL CAVITY1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.