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Hu-Friedy MFG Co., LLC. SBH5/6USC9E2Recalls & reported problems

Hu-Friedy Mfg. CO., LLC · #5/6 Barnhart Curette, USC/Suter EE2 #9 · 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 10889950102616), received between Jul 26, 2023 and Jul 26, 2023 — classified as 1 malfunction.

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.

Most reported problems

Device problems

  • Break1

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.

  • MalfunctionJul 26, 2023Break; Break

    THE USER FACILITY REPORTED THAT DURING A DENTAL PROCEDURE A PIECE OF ONE OF THE TIPS TO THEIR 5/6 BARNHART CURETTE, USC/SUTER DETACHED IN THE PATIENT'S MOUTH. THE PART WAS SURGICALLY REMOVED.

    Patient problems: Insufficient Information

    MAUDE report 17398933 ↗

Other CURETTE, PERIODONTIC devices

All CURETTE, PERIODONTIC devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.