Moses™ Moses™ 200 D/F/L LPRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07290109144566), received between May 6, 2025 and May 6, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Separation 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

Recent adverse event reports

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

• MalfunctionMay 6, 2025Thermal Decomposition of Device; Separation Problem; Thermal Decomposition of Device; Separation Problem

  IT WAS REPORTED THAT DURING THE PROCEDURE, THE LASER FIBER END BEGAN TO SMELL LIKE BURNING AND SMOKING. THE FIBER WAS REMOVED FROM THE CONSOLE, AND IT WAS VERY HOT TO THE TOUCH. THE FIBER HAD DETACHED FROM THE RUBBER COATING AND WAS CHARRED AT THE END. THE PROCEDURE WAS COMPLETED WITH ANOTHER FIBER WITHOUT PATIENT COMPLICATIONS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21971670 ↗