ATTUNE LPS 1517-60-120Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10603295491101), received between Apr 1, 2021 and Aug 3, 2026 — classified as 6 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 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjuryAug 3, 2026Adverse Event Without Identified Device or Use Problem

  It was reported that the patient experienced pain.Affected side: Left knee.

  Patient problems: Pain

  MAUDE report 50116620 ↗
• InjuryMar 18, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED DUE TO INFECTION. I&D POLY SWAP WAS PERFORMED. THERE WAS NO SURGERY DELAY OR PATIENT CONSEQUENCES. DOI: (B)(6) 2021. DOR: (B)(6) 2025. AFFECTED SIDE: RIGHT KNEE.

  Patient problems: Unspecified Infection

  MAUDE report 21635196 ↗
• InjuryAug 26, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THE PATIENT WAS REVISED AND UNDERWENT A DISTAL FEMORAL REPLACEMENT OF THE ATTUNE POLY INSERT TODAY. THE PATIENT'S PATELLA HAD DISLOCATED LATERALLY RESULTING IN THE POLY INSERT POST SLIDING OUT AND DISENGAGING FROM THE TIBIAL COMPONENT. THE DOCTOR ELECTED TO UPSIZE THE POLY AND WORK ON THE SURROUNDING TISSUE TO ENSURE THE PATELLA DOES NOT DISLOCATE AGAIN. SURGICAL DELAY WAS UNKNOWN. DOI: (B)(6) 2024. DOR: (B)(6) 2024. AFFECTED SIDE: LEFT KNEE.

  Patient problems: Joint Dislocation

  MAUDE report 20064083 ↗
• InjuryApr 29, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED DUE TO INFECTED RTKA WITH ATTUNE LPS DISTAL FEMORAL REPLACEMENT IMPLANTS. WASH OUT IRRIGATION AND DEBRIDEMENT (I&D) WITH A NEW ATTUNE LPS INSERT EXCHANGE AND NEW HINGE PIN. DOI: (B)(6) 2024. DOR: (B)(6) 2024. AFFECTED SIDE: RIGHT KNEE.

  Patient problems: Unspecified Infection

  MAUDE report 19202149 ↗
• InjuryOct 10, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT HAD A PATELLA THAT WAS NOT TRACKING AND WAS RIDING LATERALLY OUTSIDE THE DISTAL FEMORAL REPLACEMENT. SURGEON CHOSE TO SHORTEN THE CONSTRUCT BY REDUCING THE INSERT THICKNESS AND PERFORMED AN EXTENSIVE LATERAL RELEASE. THE PATELLA HAD PREVIOUSLY NOT BEEN RESURFACED AND SURGEON CHOSE TO PLACE A PATELLAR IMPLANT. TRACKING WAS RESTORED AND A MEDIAL REPAIR TO THE RETINACULUM WAS PERFORMED. NO PATIENT HARM OCCURRED NOR DEFICIENCY STATED. COMPONENTS WERE EXCHANGED OR REPLACED DUE TO REPOSITIONING OF COMPONENTS TO ENHANCE PATELLAR TRACKING. DOI: (B)(6) 2023. DOR: (B)(6) 2023. AFFECTED SIDE: RIGHT KNEE.

  Patient problems: Joint Laxity; Unspecified Tissue Injury

  MAUDE report 17907188 ↗
• InjuryApr 1, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE IMPLANTS REMOVED WERE INSERTED ON (B)(6) 2021. DER HAVE BEEN SUBMITTED ON EACH OF THESE DATES WITH RESPECTIVE CHANGES. ULTIMATELY THE GRAFT THAT WAS PLACED IN THE PATIENT BECAME INFECTED AND ALL IMPLANTS WERE REMOVED. ANTIBIOTIC BEADS AND A SPACER WAS PLACED IN THE PATIENT. NO DELAY TO SURGERY REPORTED. DOI: (B)(6) 2021 (TIBIAL TRAY, TIBIAL STEM, TIBIAL SLEEVE, AND CONTROL CABLE), DOI: (B)(6) 2021 (DISTAL FEMORAL COMPONENT, AND FEMORAL STEM), DOI: (B)(6) 2021 (FEMORAL SEGMENTAL COMPONENTS, AND TIBIAL INSERT), DOR: (B)(6) 2021, RIGHT KNEE.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 11602907 ↗