MultiLASE TFL UL600Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 08059173392278), received between Apr 18, 2025 and Apr 18, 2025 — classified as 2 injuries.

The most frequently reported specific device problem is “Application Program Freezes or Fails to Launch” (2 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 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryApr 18, 2025Application Program Freezes or Fails to Launch; Application Program Freezes or Fails to Launch

  IT WAS REPORTED THAT DURING A VETERINARY PROCEDURE (INFORMATION OF CASE DATE OR TYPE WAS NOT PROVIDED), THE DEVICE SCREEN FROZE AND COULD NOT BE RESET BY THE TEAM FORCING THEM TO ABANDON THE PROCEDURE. THE ANIMAL PATIENT WAS THEN MOVED TO A NEARBY FACILITY FOR TREATMENT. NO FURTHER INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21869606 ↗
• InjuryApr 18, 2025Device Fell; Application Program Freezes or Fails to Launch; Device Fell; Application Program Freezes or Fails to Launch

  IT WAS REPORTED THAT DURING A VETERINARY PROCEDURE (INFORMATION OF CASE DATE OR TYPE WAS NOT PROVIDED), THE DEVICE SCREEN FROZE AND COULD NOT BE RESET BY THE TEAM FORCING THEM TO ABANDON THE PROCEDURE. THE ANIMAL PATIENT WAS THEN MOVED TO A NEARBY FACILITY FOR TREATMENT. NO FURTHER INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21869605 ↗