Tornier Perform MWH685Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00846832071074), received between Sep 20, 2022 and Dec 18, 2025 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Fracture” (2 reports).

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryDec 18, 2025Fracture; Fracture

  IT WAS REPORTED THAT DURING THE GLENOID PREPARATION FOR THE AUGMENTED (CORTILOC +) IMPLANT, THE ANTI-ROTATION PEG DRILL BROKE INTO TWO PIECES. ONE PIECE CAME OUT, AND ONE PIECE REMAINED IN THE PATIENT. APPROXIMATELY 45 MINUTES WAS SPENT TRYING TO REMOVE THE REMAINING PIECE FROM THE PATIENT. X-RAY IMAGING AND ARTHROSCOPY WERE USED TO TRY TO REMOVE THE PIECE BUT WERE UNSUCCESSFUL. THE SURGEON DECIDED TO PROCEED WITH SURGERY, LEAVING ONE PIECE OF THE ANTI-ROTATION PEG DRILL IN THE PATIENT.

  Patient problems: Foreign Body In Patient; Insufficient Information

  MAUDE report 23840503 ↗
• MalfunctionSep 20, 2022Break; Fracture; Break; Fracture

  IT WAS REPORTED THAT WHEN DRILLING THE POSTERIOR PERIPHERAL HOLE, ONE OF THE QUICK RELEASE DRILL BITS SNAPPED IN HALF. THE PATIENT HAD 10 DEGREES OF RETROVERSION.

  Patient problems: Insufficient Information

  MAUDE report 15456299 ↗