Lumenis Pulse P120 30 AmpRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07290109147338), received between Sep 14, 2023 and Sep 14, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Output below Specifications” (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 16, 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.

• MalfunctionSep 14, 2023Output below Specifications; Output below Specifications

  IT WAS REPORTED THAT CONSOLE WAS FOUND TO BE FIRING WITH A LIMITED OUTPUT (LOW POWER) DURING PROCEDURE. NO ERROR CODES WERE DISPLAYED. IT WAS NOTED THAT THE FIBER AND THE BLAST SHIELD WAS CHANGED BUT THE ISSUE PERSISTED. THE PROCEDURE WAS COMPLETED WITH THIS DEVICE WITH NO PATIENT COMPLICATIONS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17745605 ↗