FullFire® Diffusing Tip Laser Probe 20414-000 (REF DTP-000-01)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00816589020618), received between Sep 29, 2017 and Sep 29, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Temperature 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 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 29, 2017Temperature Problem; Temperature Problem

  ADDITIONAL INFORMATION RECEIVED INDICATED THAT THERE WERE NO PATIENT ADVERSE EVENTS AND THAT THE PATIENT IS "ALIVE AND DOING WELL".

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 6903328 ↗