Hu-Friedy MFG Co., LLC. SH6/79E2Recalls & reported problems
Hu-Friedy Mfg. CO., LLC · H6/H7 DE Scaler, EE2 #9 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 10889950028367), received between Apr 16, 2026 and Apr 16, 2026 — classified as 1 injury.
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 16, 2026Break
CUSTOMER REPORTED THAT INSTRUMENT BROKE AND THE PATIENT STATED THEY SWALLOWED THE TIP/PIECE. PATIENT RECEIVED AN X-RAY AND THE INSTRUMENT PIECE WAS NOT VISIBLE ON X-RAY.
Patient problems: Foreign Body In Patient
MAUDE report 24903876 ↗
Other SCALER, PERIODONTIC devices
- Hu-Friedy SCNEVI4XE2Hu-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.