NUPRO® 965250Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI D0039652501), received between Jun 25, 2025 and Jun 25, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Patient-Device Incompatibility” (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.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 25, 2025Patient-Device Incompatibility; Patient-Device Incompatibility

  IN THIS EVENT IT IS REPORTED THAT NUPRO REVOLV 90D SOFT MULTI (PD) IS ALLEGED THAT PATIENT HAD AN ALLERGIC REACTION TO SOMETHING DURING THEIR CLEANING. THE HYGIENIST THINKS IT IS THE PROPHY CUP USED DURING THE POLISHING OF THE PATIENTS¿ TEETH. A DENTSPLY SIRONA NUPRO FREEDOM- REVOLVE PROPHY CUP WAS USED WITH A NON-DENTSPLY SIRONA POLISHING PASTE. PATIENT WILL SEE HER ALLERGIST IN (B)(6) 2025, AS THIS IS THE SOONEST APPOINTMENT AVAILABLE". NO INJURY WAS REPORTED FROM THE ALLEGED EVENT.

  Patient problems: Hypersensitivity/Allergic reaction

  MAUDE report 22327582 ↗