ATTUNE LPS 1517-60-218Recalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 10603295490999), received between Oct 17, 2022 and Mar 30, 2026 — classified as 8 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (4 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. 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 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• InjuryMar 30, 2026Fracture; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT EXPERIENCED PAIN AND INSTABILITY, WITH IMAGING REVEALING THAT THE INSERT HAD DISLOCATED FROM THE TIBIAL COMPONENT. UPON SURGICAL INTERVENTION, THE INSERT WAS FOUND TO BE BOTH DISLOCATED AND BROKEN. ALL FRAGMENTS WERE REMOVED AND SENT TO PATHOLOGY AS PER HOSPITAL PROTOCOL. THE FEMORAL, TIBIAL, AND PATELLAR COMPONENTS WERE EVALUATED AND FOUND TO BE WELL ALIGNED AND SOLIDLY FIXED, SO THESE WERE RETAINED. A NEW INSERT AND HINGE PIN WERE IMPLANTED, AND THE PROCEDURE WAS COMPLETED WITHOUT FURTHER NOTED ISSUES. DOI: ON (B)(6) 2025. DOR: ON (B)(6) 2026. AFFECTED SIDE: RIGHT.

  Patient problems: Joint Dislocation; Joint Laxity; Pain

  MAUDE report 24730505 ↗
• InjurySep 2, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT PATIENT EXPERIENCED A DISLOCATION. AN LPS KNEE WAS REVISED TO ADDRESS IMPLANT DISLOCATION, WHICH FOR THIS CONSTRUCT, OCCURS BETWEEN THE TIBIAL INSERT AND THE TIBIAL TRAY. THE SURGEON PERFORMED A POLY SWAP/UPSIZE. DOI: (B)(6) 2025, DOR: (B)(6) 2025, AFFECTED SIDE: LEFT KNEE.

  Patient problems: Joint Dislocation

  MAUDE report 22947351 ↗
• InjuryAug 15, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT WAS REVISED DUE TO POSSIBLE INFECTION. INCISION AND DRAINAGE WITH POLY SWAP. AFFECTED SIDE: RIGHT KNEE.

  Patient problems: Unspecified Infection

  MAUDE report 22817930 ↗
• InjuryJun 4, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED DUE TO KNEE INSTABILITY. DOI: ON (B)(6) 2022, DOR: ON (B)(6) 2024, AFFECTED SIDE: LEFT KNEE.

  Patient problems: Joint Laxity

  MAUDE report 19459435 ↗
• InjuryOct 2, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THE PATIENT WAS REVISED AS HE FELL AND HYPER FLEXED HIS KNEE AND DISLOCATED THE HINGE INSERT. SURGICAL DELAY WAS UNKNOWN. DOI: (B)(6) 2023, DOR: (B)(6) 2023, AFFECTED SIDE: LEFT KNEE.

  Patient problems: Fall; Joint Dislocation; Joint Laxity

  MAUDE report 17851208 ↗
• InjurySep 13, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  FAILURE OF LPS MEDICAL RECORD WAS REVIEWED BY CLINICIAN. ON (B)(6) 2023, THE PATIENT WAS REVISED TO ADDRESS DISLOCATION OF THE TIBIAL TRAY AND INSERT. IT WAS NOTED THAT THIS EVENT WAS DUE TO CONDITION OF THE SOFT TISSUE. THE FEMORAL COMPONENT WAS ALSO REVISED FOR UNKNOWN REASON. FOLLOW-UP IS BEING CONDUCTED.

  Patient problems: Joint Dislocation; Joint Laxity; Loss of Range of Motion; Unspecified Tissue Injury

  MAUDE report 17739631 ↗
• InjurySep 13, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANTS WERE REMOVED DUE TO INFECTION. THE POLY WAS COMPLETELY REMOVED. THE FEMUR WAS LEFT IN BUT THE PIN (THAT¿S INCLUDED IN THE FEMUR PACKAGING) WAS REMOVED/REPLACED. DOI: (B)(6) 2022 DOR: (B)(6) 2023 AFFECTED SIDE : RIGHT KNEE.

  Patient problems: Unspecified Infection

  MAUDE report 17735602 ↗
• InjuryOct 17, 2022Fracture; Fracture

  IT WAS REPORTED THAT THE PATIENT CURRENTLY HAS A DEPUY LPS DISTAL FEMUR AND ATTUNE TIBIA IN PLACE. PATIENT FRACTURED THE METAL POST IN ATTUNE LPS XSM 18MM INSERT FOR THE SECOND TIME. SURGEON REPLACED WITH NEW POLY ON (B)(6) 2022. NOT SURE DATES OF ORIGINAL SURGERY OR FIRST REVISION DUE TO FRACTURED INSERT. DOI: UNKNOWN; DOR: (B)(6) 2022; AFFECTED SIDE: LEFT KNEE.

  Patient problems: Insufficient Information

  MAUDE report 15614385 ↗