LPS 1987-25-414Recalls & reported problems
Depuy (Ireland) · LPS STEM - STRAIGHT 14mm x 125mm CEMENTED · Class 2 · Implant
All models of LPS (113)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295079194), received between Mar 23, 2021 and Mar 23, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (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 16, 2026.
Most reported problems
Device problems
- Loss of or Failure to Bond1
Patient problems
- Discomfort1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 23, 2021Loss of or Failure to Bond; Loss of or Failure to Bond
PATIENT RECEIVED LEFT KNEE REVISION OF THE STEM AND FEMORAL COMPONENT TO TREAT THIGH DISCOMFORT ASSOCIATED WITH LOOSENING OF THE COMPONENTS AT THE CEMENT TO IMPLANT INTERFACE. SURGEON SAID PATIENT HAD THEIR KNEE REVISED BACK ON (B)(6) 2020. SURGEON PREFORMED THE REVISION AND JUST EXCHANGED THE POLY FROM A 26MM TO 28MM. SURGEON DIDN'T HAVE ACCESS TO THE PREVIOUS PROCEDURE DATES PRIOR TO SURGEON REVISION. DOI: (B)(6) 2019 (STEM AND FEMORAL). DOI: (B)(6) 2020 (INSERT AND HINGE PIN). DOR: (B)(6) 2021; LEFT KNEE.
Patient problems: Discomfort
MAUDE report 11554764 ↗
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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