Arthrex® AR-18716P-22Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867313545), received between Jun 23, 2020 and Jun 23, 2020 — 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 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 23, 2020Break; Difficult to Remove

  IT WAS REPORTED THAT ONE OF THE LITTLE PRONGS ON THE AR-18716P-22 PLATE BROKE OFF IN THE TOE BONE AND WAS NOT RETRIEVED. THE CASE WAS A TOE OSTEOTOMY ON THE LEFT BIG TOE. ANOTHER PLATE WAS USED TO COMPLETE THE CASE.

  Patient problems: Device Embedded In Tissue or Plaque

  MAUDE report 10185011 ↗