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Lares Research 757 ProStyle SF SRecalls & reported problems

Lares Research · High-speed Handpiece, 757 ProStyle SF, Swivel · 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 D950131412220), received between Aug 31, 2023 and Aug 31, 2023 — 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Mechanical Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionAug 31, 2023Mechanical Problem; Mechanical Problem

    DR SENT IN DEVICE WITH NOTE THAT A BUR HAD COME OUT DURING PROCEDURE. THE BUR WAS NOT SWALLOWED BY THE PAITENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17664696 ↗

Other Handpiece, Air-Powered, Dental devices

All Handpiece, Air-Powered, Dental devices →

Sources and updates

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