ATTUNE LPS 1517-60-314Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295490876), received between Jan 25, 2023 and Jan 30, 2023 — classified as 2 injuries.

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.

• InjuryJan 30, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT HAD A REVISION KNEE PLACED ON (B)(6) 2022 AND WAS WASHED OUT WITH PIN AND POLY EXCHANGED ON (B)(6) 2023. PATIENT HAD A STATIC SPACER PLACED DUE TO INFECTION. THERE WAS NO PATIENT HARM OCCURRED. DOI: (B)(6) 2022. DOR: (B)(6) 2023. AFFECTED SIDE: LEFT KNEE.

  Patient problems: Unspecified Infection

  MAUDE report 16269685 ↗
• InjuryJan 25, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT PRESENTED IN EMERGENCY ROOM WITH A DRAINING KNEE. PATIENT BROUGHT TO OPERATING ROOM FOR I&D WITH POLY EXCHANGE AND PLACEMENT OF ANTIBIOTIC RESORBABLE BEADS. THE HINGE PIN WAS EXCHANGED FROM THE LISTED FEMORAL COMPONENT BUT THE FEMORAL COMPONENT WAS RETAINED. INFECTION CANNOT BE CONFIRMED AT THIS TIME. NO PATIENT HARM OCCURRED. NO SURGICAL DELAY WAS THERE. DOI: (B)(6) 2022. DOR: (B)(6) 2023. AFFECTED SIDE: LEFT KNEE.

  Patient problems: Fluid Discharge; Unspecified Infection

  MAUDE report 16239642 ↗