foret Ø2,5 à embout AO 250855Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03661489508554), received between Nov 12, 2025 and Nov 12, 2025 — 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 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.

• MalfunctionNov 12, 2025Fracture; Fracture

  PERFORMING INTRAMEDULLARY NAILING OF A LONG OPEN FRACTURE OF THE UPPER THIRD OF THE HUMERUS. USE OF A SHORT NAIL LOCKED WITH TWO PROXIMAL SCREWS AND A DISTALE SCREW. DURING SURGERY THE DRILL WAS USED AND THEN SENT TO THE STERILISATION DEPARTMENT. THE STERILISATION DEPARTMENT NOTICED THAT THE DISTAL END OF THE DRILL WAS MISSING. THE OPERATING THEATRE PERFORMED A CONTOL X-RAY, DURING WHICH THE TIP WAS NOT FOUND. IT IS IMPOSSIBLE TO DETERMINE WITH CERTAINTY THAT THE TIP HAS NOT REMAINED IN THE PATIENT'S BODY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23534331 ↗