Tornier Perform MWM066Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00846832082896), received between Dec 17, 2025 and May 1, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Fracture” (3 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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 1, 2026Fracture

  DURING USE, THE SLAPHAMMER FRACTURED WHILE ENGAGED WITH A SIZE 4 TRIAL STEM. ADDITIONALLY, TWO SIZE 2 SIZER DISCS WERE NOTED TO BE BROKEN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25059412 ↗
• MalfunctionMar 17, 2026Fracture

  IT WAS REPORTED THAT, THE TIP OF THE SLAP HAMMER SCREW BROKE OFF. PART OF THE SCREW REMAINS INSIDE THE SIZE 3 COMPACTOR. OCCURRED DURING COMPACTOR REMOVAL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24616787 ↗
• MalfunctionDec 17, 2025Fracture; Fracture

  IT WAS REPORTED THAT, DURING STEM REMOVAL, THE SCREW AT THE TIP OF THE SLAP HAMMER BROKE. NO FURTHER INFORMATION WAS PROVIDED.

  Patient problems: Foreign Body In Patient; No Clinical Signs, Symptoms or Conditions

  MAUDE report 23829829 ↗