TRUMATCH ATTUNE 420945Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295431794), received between Dec 22, 2017 and Feb 19, 2019 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Fracture” (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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 19, 2019Incorrect Measurement; Incorrect Measurement

  IT WAS REPORTED THAT THE SURGEON USED A DIFFERENT SIZE TIBIA THAN THE TRUMATCH PLAN SUGGESTED. A SIZE THREE (3) TIBIA WAS USED INSTEAD OF A SIZE TWO (2). THE RESECTION LEVEL WAS NOT ADJUSTED AND DID MATCH THE PLAN.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8350144 ↗
• MalfunctionDec 22, 2017Fracture; Fracture

  IT WAS REPORTED THAT ONE OF THE ARMS FROM THE TIBIAL CUTTING BLOCK BROKE WHILE SURGEON WAS CUTTING THE PROXIMAL TIBIA. BOTH PIECES WERE RETRIEVED AND IT DID NOT EXTEND THE CASE TIME.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7141676 ↗