LPS 1987-16-215Recalls & reported problems
Depuy (Ireland) · LPS FEMORAL STEM BOWED 16.5mm x 150mm POROCOAT · Class 2 · Implant
All models of LPS (113)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295078890), received between May 30, 2019 and Nov 11, 2025 — classified as 3 injuries.
The most frequently reported specific device problem is “Migration” (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.
Reports received per month
Most reported problems
Device problems
- Migration2
- Loss of Osseointegration1
- Loss of or Failure to Bond1
- Osseointegration Problem1
Patient problems
- Inadequate Osseointegration1
- Insufficient Information1
- No Code Available1
- Physical Asymmetry1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryNov 11, 2025Migration; Migration
IT WAS REPORTED THAT PATIENT HAD A DISTAL FEMUR REPLACEMENT ON (B)(6) 2025. PATIENT RIGHT FEMORAL COMPONENT SUBSIDED AFTER WE PUT IN A POROUS STEM AFTER THREE MONTHS. SURGEON REVISED JUST THE LPS DISTAL FEMUR USING A CEMENTED. DOI: (B)(6) 2025. DOR: (B)(6) 2025. AFFECTED SIDE: RIGHT KNEE.
Patient problems: Insufficient Information
MAUDE report 23526931 ↗InjuryMay 14, 2024Osseointegration Problem; Migration; Osseointegration Problem; Migration
IT WAS REPORTED THAT THE PATIENT HAD A LPS SEGMENTAL DFR IN 2020. SINCE THAT TIME THE STEM HAS LOOSENED AND SHORTEN. THE LOOSENING INTERFACE WAS NON-CEMENTED. THE SURGERY WAS TO REMOVE THE LOOSE IMPLANT AND CEMENT IN A NEW SEGMENTAL DFR. THERE WAS NO INFECTION OR DELAYS OR BROKEN EQUIPMENT. DOI: (B)(6) 2020. DOR: (B)(6) 2024. AFFECTED SIDE: RIGHT KNEE.
Patient problems: Physical Asymmetry
MAUDE report 19312310 ↗InjuryMay 30, 2019Loss of or Failure to Bond; Loss of Osseointegration; Loss of or Failure to Bond; Loss of Osseointegration
LPS FEMORAL COMPONENTS REVISED DUE TO THE STEM BECOMING LOOSE AND THE FEMORAL COMPONENT ROTATING.
Patient problems: Inadequate Osseointegration; No Code Available
MAUDE report 8653556 ↗
Other Prosthesis, hip, semi-constrained, metal/polymer, cemented devices
- NA 1365-51-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented753 reports
- NA 1365-50-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented412 reports
- ARTICUL/EZE 1365-21-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall280 reports
- ARTICUL/EZE 1365-11-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 death262 reports
- LFIT 6260-9-236Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, cemented256 reports
- PINNACLE GRIPTION 1217-32-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented2 deaths239 reports
- ELEOS™ 25002111EOnkos Surgical, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented3 deaths230 reports
- Novation 130-36-52Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2 recalls124 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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