LPS 1987-26-416Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295079316), received between Sep 14, 2018 and Feb 20, 2025 — classified as 4 injuries.

The most frequently reported specific device problem is “Osseointegration Problem” (2 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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 20, 2025Osseointegration Problem; Osseointegration Problem

  IT WAS REPORTED THAT PATIENT WAS REVISED DUE TO LOSE FEMORAL STEM/CONSTRUCT. THE 17.5X125 MM STRAIGHT POROUS STEM WAS LOOSE AND THE LOOSENING INTERFACE WAS NON-CEMENTED. NO BROKEN PIECES. ALL COMPONENTS RETRIEVED. MINIMAL SURGICAL DELAY WHEN EXPLANTING STEM. DOI: (B)(6) 2023, DOR: (B)(6) 2025, AFFECTED SIDE: LEFT HIP.

  Patient problems: Inadequate Osseointegration

  MAUDE report 21425785 ↗
• InjuryAug 17, 2023Osseointegration Problem; Osseointegration Problem

  IT WAS REPORTED THAT PATIENT HAD THE KNEE REPLACEMENT ON (B)(6) 2021 BY THE SURGEON WHERE SURGEON IMPLANTED AN LPS STEM, LPS DISTAL FEMUR, LPS INSERT, AND A MBT TRAY. SURGEON DECIDED TO REVISE THE CONSTRUCT DUE TO KNEE PAIN OF THE PATIENT. DURING THE REVISION IT WAS DISCOVERED THAT THE LPS FEMORAL PRESS FIT CEMENTLESS STEM WAS LOOSE. A LONGER STEM WAS TRIALED AND THEN A NEW CONSTRUCT WAS IMPLANTED. THE MBT TIBIAL TRAY WAS WELL FIXED. DOI: (B)(6) 2021. DOR: (B)(6) 2023. AFFECTED SIDE: RIGHT KNEE.

  Patient problems: Inadequate Osseointegration; Pain

  MAUDE report 17563308 ↗
• InjuryMay 6, 2020Loss of Osseointegration; Loss of Osseointegration

  THE PATIENT WAS REVISE TO ADDRESS PAIN IN FEMUR AND LOOSENING OF UNKNOWN COMPONENT. IMPLANT HAD FIBROUS INGROWTH. DOI: (B)(6) 2017. DOR: (B)(6) 2020; RIGHT KNEE.

  Patient problems: Inadequate Osseointegration; No Code Available; Pain

  MAUDE report 10030384 ↗
• InjurySep 14, 2018Loose or Intermittent Connection; Loose or Intermittent Connection

  THE PATIENT WAS REVISED TO ADDRESS LOOSENING OF FEMORAL STEM AND FEMUR AT BONE TO IMPLANT INTERFACE. DOI: UNKNOWN, DOR: (B)(6) 2018, UNKNOWN SIDE.

  Patient problems: Inadequate Osseointegration

  MAUDE report 7877248 ↗