Arthrex® AR-1204F-110Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867004481), received between Feb 14, 2022 and Feb 14, 2022 — classified as 1 injury.

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.

• InjuryFeb 14, 2022Break

  IT WAS REPORTED THAT DURING AN ANTERIOR CRUCIATE LIGAMENT SURGERY THE FLIPCUTTER WAS DAMAGED WHEN DRILLING THE TIBIAL TUNNEL. NO PART OF THE DEVICE BROKE OFF. THE SURGERY WAS FINISHED SUCCESSFULLY WITH A RECALIBRATION OF THE GRAFT TO DIAMETER 10 (TIBIAL PORTION) AND THE USE OF A FLIP CUTTER N° 10 WITHOUT FURTHER PROBLEMS. IT WAS NOT NECESSARY TO SWITCH THE SURGICAL TECHNIQUE OR DO A SECOND SURGERY. ACCORDING TO THE PROVIDED INFORMATION A PATIENT HARM OCCURRED. NO FURTHER INFORMATION RECEIVED.

  Patient problems: Insufficient Information

  MAUDE report 13527102 ↗