Hu-Friedy SCNEVI4XE2Recalls & reported problems
Hu-Friedy Mfg. CO., LLC · #4 Nevi Scaler Post DE,EE2, Ergo Handle · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889950127237), received between Dec 31, 2025 and Dec 31, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Sharp Edges” (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
- Sharp Edges1
Patient problems
- Laceration(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 31, 2025Sharp Edges; Sharp Edges
USER REPORTED THAT THERE WAS A PIECE OF METAL STICKING OUT OF THE SCALER HANDLE. METAL POKED THROUGH USER'S GLOVES.
Patient problems: Laceration(s)
MAUDE report 23933703 ↗
Other SCALER, PERIODONTIC devices
- Hu-Friedy MFG Co., LLC. SH6/79E2Hu-Friedy Mfg. CO., LLC · SCALER, PERIODONTIC1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.