LPS 1987-16-315Recalls & reported problems
Depuy (Ireland) · LPS FEMORAL STEM BOWED 16.5mm x 200mm POROCOAT · Class 2 · Implant
All models of LPS (113)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295078951), received between Jan 31, 2018 and Jun 23, 2023 — classified as 4 injuries.
The most frequently reported specific device problem is “Failure to Osseointegrate” (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
Device problems
- Appropriate Device Problem Term/Code Not Available1
- Failure to Osseointegrate1
- Loose or Intermittent Connection1
- Loss of Osseointegration1
- Osseointegration Problem1
Patient problems
- Inadequate Osseointegration4
- Pain2
- No Code Available1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryJun 23, 2023Osseointegration Problem; Osseointegration Problem
PATIENT WAS REVISED DUE TO LOOSENING OF THE FEMORAL STEM AT THE BONE TO IMPLANT INTERFACE. DOI: (B)(6) 2023. DOR: (B)(6) 2023. AFFECTED SIDE: LEFT KNEE.
Patient problems: Inadequate Osseointegration
MAUDE report 17190480 ↗InjuryDec 26, 2018Failure to Osseointegrate; Failure to Osseointegrate
THE PATIENT WAS REVISED TO ADDRESS DISTAL FEMORAL REPLACEMENT FOR PAIN AND LOOSENING OF FEMORAL STEM AT THE BONE TO IMPLANT INTERFACE.
Patient problems: Inadequate Osseointegration; No Code Available; Pain
MAUDE report 8197218 ↗InjuryOct 31, 2018Loose or Intermittent Connection; Appropriate Device Problem Term/Code Not Available; Loose or Intermittent Connection; Appropriate Device Problem Term/Code Not Available
PATIENT WAS REVISED TO ADDRESS LOOSENING OF THE FEMORAL STEM.
Patient problems: Inadequate Osseointegration
MAUDE report 8024107 ↗InjuryJan 31, 2018Loss of Osseointegration; Loss of Osseointegration
PATIENT WAS REVISED TO ADDRESS PAIN IN THE MID THIGH AND LOOSENING OF THE FEMORAL COMPONENT AND STEM AT BONE TO IMPLANT INTERFACE. IT WAS ALSO REPORTED THAT THE IMPLANTS WERE REMOVED AND REVISED USING CEMENTED IMPLANTS. THE POLY PORTION OF THE PATELLA WAS ALSO REPLACED. DOI: 2014; DOR: (B)(6) 2018; LEFT HIP.
Patient problems: Inadequate Osseointegration; Pain
MAUDE report 7230218 ↗
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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