LPS 1987-26-415Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295079309), received between Aug 14, 2020 and Jun 24, 2026 — 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 16, 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.

• InjuryJun 24, 2026Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT HAD A PRIOR DISTAL FEMUR REPLACEMENT AND THE FEMUR FRACTURED. DOI: UNKNOWN. DOR: (B)(6) 2026. AFFECTED SIDE: RIGHT KNEE.

  Patient problems: Limb Fracture

  MAUDE report 25612473 ↗
• InjuryFeb 26, 2025Osseointegration Problem; Migration; Osseointegration Problem; Migration

  IT WAS REPORTED THAT PATIENT WAS REVISED DUE TO SUBSIDENCE AND LOOSENING OF THE FEMORAL STEM AT THE BONE TO IMPLANT INTERFACE. SURGEON REMOVED ALL FEMORAL COMPONENTS AND REPLACED WITH CEMENTED IMPLANTS. AFFECTED SIDE: LEFT KNEE.

  Patient problems: Inadequate Osseointegration

  MAUDE report 21472570 ↗
• InjuryFeb 1, 2023Osseointegration Problem; Osseointegration Problem

  PATIENT WAS REVISED DUE TO LOOSENING OF THE POROUS LPS STEM (NON CEMENTED) AND WAS REVISED LEAVING THE WELL FIXED TIBIAL COMPONENTS IN PLACE. NO PATIENT HARM OCCURRED. THERE WAS NO SURGICAL DELAY. DOI- (B)(6) 2018. DOR- (B)(6) 2023. AFFECTED SIDE- RIGHT HIP.

  Patient problems: Inadequate Osseointegration

  MAUDE report 16277040 ↗
• InjuryAug 14, 2020Loss of Osseointegration; Loss of Osseointegration

  PATIENT WAS REVISED DUE TO FALL AND LOOSENING OF THE FEMUR & STEM COMPONENT AT THE BONE TO IMPLANT INTERFACE. CEMENT MANUFACTURER USED WAS UNKNOWN. PATIENT HAD LPS IMPLANTED IN (B)(6) 2019. PATIENT WAS REVISED USING CEMENTED LPS STEM. DOI: (B)(6) 2019 DOR: (B)(6) 2020 RIGHT KNEE.

  Patient problems: Inadequate Osseointegration; No Code Available

  MAUDE report 10410593 ↗