Dornier MedTech 270 Micron Single Use (REF HLFD0270C)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810116020003), received between Jun 9, 2020 and Jun 9, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (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.

• MalfunctionJun 9, 2020Fracture; Fracture

  COMPLAINT INFORMATION WAS RECEIVED DETAILING TWO UNITS OF HOLMIUM FIBER. THE FIRST UNIT IDENTIFIED WAS NOTED TO BE "BENT ON THE TIP" PRIOR TO USE. THE SECOND FIBER WAS IDENTIFIED TO HAVE "BROKE INSIDE THE PATIENT". THE CUSTOMER STATED, "THIS WAS FROM A BOX THAT HAD BEEN OPENED BEFORE. IT WAS THESE TWO LASER FIBERS LEFT IN IT". NO REPORTS OF INJURY OR PATIENT COMPLICATION WAS REPORTED TO DORNIER MEDTECH AMERICA.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 10135638 ↗