ATTUNE 2504-40-207Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295439813), received between Oct 17, 2019 and Apr 19, 2021 — classified as 2 malfunctions.

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

• MalfunctionApr 19, 2021Material Twisted/Bent; Material Twisted/Bent

  IT WAS REPORTED THAT "ONE OF THE HOLES ON THE FRONT OF THE FEMUR THAT ALLOWS THE BOX TO THREAD IN THE STRIPPED. IT WON¿T ALLOW THE BOX TO SEE IT OR EVER SCREW IN. THE SURGERY WAS NOT DELAYED AND THE PATIENT HAD NOTHING LEFT IN THEM."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11685654 ↗
• MalfunctionOct 17, 2019Corroded; Corroded

  IT WAS REPORTED THAT THE INSTRUMENTS APPEAR TO HAVE RUST ON THEM. NOTHING LEFT IN PATIENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9203884 ↗