LPS 1987-15-213Recalls & reported problems
Depuy (Ireland) · LPS FEMORAL STEM BOWED 13mm x 150mm CEMENTED · Class 2 · Implant
All models of LPS (113)
Data updated Oct 18, 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 10603295078753), received between Sep 22, 2017 and Sep 22, 2017 — classified as 1 injury.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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
- Improper or Incorrect Procedure or Method1
- Loss of or Failure to Bond1
Patient problems
- Osteolysis1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 22, 2017Loss of or Failure to Bond; Improper or Incorrect Procedure or Method; Loss of or Failure to Bond; Improper or Incorrect Procedure or Method
PATIENT WAS REVISED TO ADDRESS PAIN, OSTEOLYSIS AND LOOSENING OF THE FEMORAL STEM AND TIBIAL STEM AT THE CEMENT TO IMPLANT INTERFACE. CEMENT MANUFACTURER IS UNKNOWN. UPDATE 8/24/2017 AND 8/30/2017 DER AND RECORDS REVIEWED FOR REPORTABILITY. IT WAS IDENTIFIED AND CONFIRMED WITH DEPUY PRODUCT ENGINEER FOR LPS SYSTEM THAT THE USAGE OF THE LE INTRCL STR D TAIL ASSM 55MM WITH LPS CEMENTED STEM 12X125MM STR AND LPS CEM FEM STEM 13X150MM BOW AS A CONSTRUCT ACROSS THE PATIENT'S KNEE JOINT (STEM CEMENTED IN DISTAL FEMUR AND STEM CEMENTED IN PROXIMAL TIBIA, WITH THE LE INTRCL STR D TAIL ASSM 55MM BRIDGING THE KNEE JOINT) TO FUNCTIONALLY FUSE THE KNEE JOINT (SEE INCLUDED X-RAYS) IS AN OFF LABEL USE OF THESE PRODUCTS AND POSSIBLY THE REASON FOR THEIR FAILURE, REQUIRING REVISION SURGERY. COMPLAINT UPDATED ON: 9/21/2017.
Patient problems: Osteolysis; Pain
MAUDE report 6886675 ↗
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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