Arthrex® AR-1344SE-15Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867013346), received between Jul 25, 2022 and Jul 25, 2022 — classified as 1 malfunction.

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

• MalfunctionJul 25, 2022Break; Power Problem

  KNEE SCORPIONS STOPPED WORKING AND 1 X ELEVATOR BROKE DURING A PROCEDURE. THE PROCEDURE WAS COMPLETED USING ANOTHER KNEE SCORPION AND ELEVATOR. NO PATIENT HARM.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15093824 ↗