Arthrex® AR-5025TDC-26Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867034976), received between Oct 12, 2016 and Oct 12, 2016 — classified as 1 injury.

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

• InjuryOct 12, 2016Bent; Material Fragmentation

  IT WAS REPORTED THAT WHILE DRILLING IN THE MEDIAL CONDYLE FOR A COMPRESSION SCREW FOR A KNEE SCOPE-OCD REPAIR, PIECES OF THE DRILL BROKE OFF. WHEN THE DRILL WAS REMOVED THE K-WIRE WAS LODGED IN THE CANNULATION. IT WAS BENT AND REMOVED ON THE BACK TABLE. IT WAS NOT REALIZED UNTIL THE CONCLUSION OF DRILLING THAT THE FRAGMENTS WERE MISSING. THE FRAGMENTS WERE LEFT IN THE BOTTOM OF THE SOCKET AND WERE CONFIRMED BY X-RAYS. IT WAS REPORTED THAT THE RESULT OF THE CASE WAS UNAFFECTED BY THE DRILL FRAGMENTS AND THE SURGEON WAS SATISFIED WITH THE COMPRESSION AND FIXATION OF THE CHONDRAL DEFECT.

  Patient problems: Device Embedded In Tissue or Plaque

  MAUDE report 6022130 ↗