Hu-Friedy MFG Co., LLC. SRP1/2R9E2Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10889950102838), received between Aug 27, 2026 and Aug 27, 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 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.

• InjuryAug 27, 2026Break

  During a dental hygiene procedure, a student clinician was treating a Class IV periodontal patient using a Gracey 1/2 curette when the working tip fractured and separated from the instrument. The tip was immediately recovered. As a precautionary measure, an X-ray was taken to verify that no fragment remained embedded in the patient's subgingival tissue. The X-ray confirmed that no fragment was retained.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50478563 ↗