Lares Research 557 ProStyle SF Lite SLRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI D950131242220), received between Aug 9, 2023 and Jul 23, 2025 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Mechanical Problem” (3 reports).

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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 23, 2025Mechanical Problem; Mechanical Problem

  DR. SENT HANDPIECE IN FOR SERVICE WITH A NOTE THAT THE BUR HAD COME OUT DURING A PROCEDURE. THE BUR WAS RETRIEVED AND NO INJURY WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22576835 ↗
• MalfunctionJul 23, 2025Mechanical Problem; Mechanical Problem

  DR. SENT HANDPIECE IN FOR REPAIR WITH A NOTE STATING THE HEAD CAP HAD COME OFF IN A PATIENT'S MOUTH. THE HEAD CAP WAS RETRIEVED AND NO INJURY WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22576802 ↗
• MalfunctionAug 9, 2023Mechanical Problem; Mechanical Problem

  HANDPIECE WAS SENT IN BY CUSTOMER WITH A NOTE INDICATING A PIECE OF THE TURBINE HAD FLOWN OUT DURING PROCEDURE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17494976 ↗