ATTUNE 1517-10-726Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295056225), received between May 7, 2021 and Jun 23, 2026 — classified as 4 injuries.

The most frequently reported specific device problem is “Unintended Movement” (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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryJun 23, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT WAS REVISED DUE TO PAIN. AFFECTED SIDE: RIGHT KNEE.

  Patient problems: Pain

  MAUDE report 25594309 ↗
• InjuryOct 10, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  ADDITIONAL INFORMATION WAS RECEIVED: CLINICAL ADVERSE EVENT RECEIVED FOR REVISION DUE TO INFECTION, DEVICE RELATED: NO INFORMATION PROVIDED, PROCEDURE RELATED: NO INFORMATION PROVIDED, DATE OF EVENT: SEPTEMBER 6, 2024, DATE OF IMPLANT: (B)(6) 2024, DATE OF REVISION: (B)(6) 2024, DEVICE LOCATION: LEFT.

  Patient problems: Unspecified Infection

  MAUDE report 20417324 ↗
• InjuryAug 14, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  ADDITIONAL INFORMATION WAS RECEIVED: NO. THERE WAS NO SURGICAL DELAY.

  Patient problems: Unspecified Infection

  MAUDE report 19982488 ↗
• InjuryMay 7, 2021Unintended Movement; Unintended Movement

  THE PATIENT WAS REVISED TO ADDRESS POLY SPIN OUT DUE TO THE GAP BETWEEN THE FEMUR AND TIBIA BEING TOO LARGE. SURGEON IMPLANTED A HINGE WITH THICK TRAY TO CLOSE THE JOINT SPACE. NO SURGICAL DELAY HAS BEEN REPORTED. DOI: (B)(6) 2020. DOR: (B)(6) 2021; LEFT KNEE.

  Patient problems: Joint Laxity

  MAUDE report 11791130 ↗