ATTUNE 2517-10-818Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295481904), received between May 30, 2019 and May 30, 2019 — classified as 1 malfunction.

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 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.

• MalfunctionMay 30, 2019Break; Break

  LEFT TIBIAL CUTTING BLOCK WAS DAMAGED IN CASE. RESIDENT PINED TIBIAL CUTTING BLOCK WITH PIN AND STARTED THE DRILLING AT AN ANGLE. THIS STRIPPED THE PIN AND JAMMED IT IN ONE OF THE PIN HOLES LOCATED ON THE CUTTING BLOCK. THIS ADDED ROUGHLY 2-3 MINUTES TO THE CASE. THEY WERE UNABLE TO REMOVE THE PIN FROM THE CUTTING BLOCK AFTER THE CUT HAD BEEN MADE. THEY WERE EVENTUALLY ABLE TO TWIST THE BLOCK AND PIN OUT OF THE PATIENT. AN INSERT HANDLE AND INSERT WERE DAMAGED IN THE CASE. THE SURGEON MADE A CLEAN UP CUT WITH INSERT AND HANDLE IN PLACE. BOTH THE INSERT AND INSERT HANDLE WERE REPORTED TO BE BROKEN.

  Patient problems: Not Applicable

  MAUDE report 8653641 ↗