ATTUNE LPS 1517-60-220Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295491002), received between Nov 13, 2020 and Dec 8, 2025 — classified as 2 injuries.

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

• InjuryDec 8, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT HAD SWELLING IN THE KNEE; MUCH FLUID DRAINED FROM JOINT UPON INCISION AND TISSUE WAS BLACK (PRESUMABLY FROM METALLOSIS). THE HINGE PROSTHESIS WAS LARGELY UNSUPPORTED BY BONE AND IT APPEARS THAT THE HINGE FEMUR WAS MOVING WITHIN THE SLEEVE, CREATING METAL DEBRIS AND INSTABILITY. LOOSENING COMPONENT AT THE BONE TO IMPLANT INTERFACE. DOI: ON (B)(6) 2023, DOR: ON (B)(6) 2025, AFFECTED SIDE: LEFT KNEE.

  Patient problems: Bone Notching; Fluid Discharge; Foreign Body Reaction; Joint Laxity; Swelling/ Edema

  MAUDE report 23749394 ↗
• InjuryNov 13, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT FELL AND TORN MULTIPLE EXTENSOR MECHANISMS. POLY DISLOCATED. DOI: (B)(6) 2020, DOR: (B)(6) 2020, LEFT KNEE.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Fall; Joint Dislocation; No Code Available

  MAUDE report 10835819 ↗