Perfect Finish 1:1 Contra Angle with push-button latch headRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI D950116310), received between Dec 22, 2025 and Dec 22, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Mechanical Problem” (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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 22, 2025Mechanical Problem; Mechanical Problem

  DR. SENT EMAIL AND INDICATED HE WAS WORKING ON A PEDIATRIC PATIENT WHEN THE HEAD CAP CAME OFF HIS LOW-SPEED CONTRA ANGLE. PATIENT WAS REFERRED TO HAVE A CHEST X-RAY TO RULE OUT INGESTION OR ASPIRATION OF PARTS. FROM DEVICE PHOTO SENT BY DR. ALL PARTS ARE ACCOUNTED FOR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23865688 ↗