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Hu-Friedy SG7/877Recalls & reported problems

Hu-Friedy Mfg. CO., LLC · #7/8 Gracey Curette, #7 Handle, Green · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 10889950095598), received between Jun 17, 2022 and Jun 17, 2022 — 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

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.

  • MalfunctionJun 17, 2022Break; Break

    THE USER FACILITY REPORTED THAT THE TIP OF THEIR GRACEY CURETTE DETACHED IN THE PATIENT'S MOUTH DURING A DENTAL PROCEDURE AND THE PATIENT SWALLOWED THE TIP. THE TIP OF THE GRACEY CURETTE WAS REMOVED FROM THE PATIENT DURING A SUBSEQUENT ENDOSCOPIC PROCEDURE.

    Patient problems: Foreign Body In Patient

    MAUDE report 14733340 ↗

Other CURETTE, PERIODONTIC devices

All CURETTE, PERIODONTIC devices →

Sources and updates

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