LCS 1178-20-025Recalls & reported problems
Depuy Orthopaedics, Inc. · LCS TIBIAL INSERT MENISCAL BEARING STD 10mm · Class 3 · Implant
All models of LCS (45)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10603295007760), received between Aug 9, 2017 and Oct 1, 2024 — classified as 4 injuries, 1 malfunction.
The most frequently reported specific device problem is “Naturally Worn” (5 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
- Naturally Worn5
- Off-Label Use1
Patient problems
- Insufficient Information2
- No Clinical Signs, Symptoms or Conditions1
- No Code Available1
- No Information1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryOct 1, 2024Naturally Worn; Naturally Worn
ADDITIONAL INFORMATION WAS RECEIVED: A. WAS THERE ANY ADVERSE CONSEQUENCES THAT AFFECTED THE PATIENT BECAUSE OF THE REPORTED EVENT? - NO. B. WHAT WAS THE ALLEGATION AGAINST THE REPORTED PRODUCT? ¿ NOT SURE. C. HAS THERE BEEN A REMOVAL/ REVISION SURGERY? - NO. D. WHAT IS THE AFFECTED SIDE INVOLVED IN THIS EVENT AND WHAT WAS THE EVENT DATE? - INFORMATION BELOW. JOINT: KNEE. SIDE: LEFT. PATIENT PROCEDURE: PRIMARY TOTAL PROSTHETIC REPLACEMENT NOT USING CEMENT OP DATE: (B)(6) 2009.
Patient problems: Insufficient Information
MAUDE report 20344521 ↗InjurySep 5, 2023Naturally Worn; Naturally Worn
SURGEON IS ORDERING A PATIENT SPECIFIC LCS KNEE POLY-INLAY FOR A PLANNED REVISION BECAUSE OF NORMAL AND EXPECTED PE-WEAR LEFT SIDE. DOI: 2005. DOR: PLANNED AS SOON AS PATIENT SPECIFIC IMPLANT WILL BE MANUFACTURED BY DEPUY IN AUTUMN 2023. THERE HAS BEEN NO ALLEGATION OF ANY PRODUCT DEFICIENCY. DOI: (B)(6) 2005, DOE: PENDING, AFFECTED SIDE: UNKNOWN.
Patient problems: Insufficient Information
MAUDE report 17681817 ↗MalfunctionMar 9, 2021Off-Label Use; Naturally Worn; Off-Label Use; Naturally Worn
ADDITIONAL INFORMATION RECEIVED STATES THAT THERE WAS A SURGICAL DELAY OF 20 MINUTES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11446189 ↗InjuryOct 22, 2020Naturally Worn; Naturally Worn
InjuryAug 9, 2017Naturally Worn; Naturally Worn
DER STATES THAT STD 10 MM MENISCAL BEARINGS AND ST PATELLA POLY EXCHANGED FOR WEAR.
Patient problems: No Information
MAUDE report 6778274 ↗
Other Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing devices
- ATTUNE 1506-10-005Depuy (Ireland) · Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing442 reports
- ATTUNE 1506-10-004Depuy (Ireland) · Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing442 reports
- ATTUNE 1518-20-038Depuy (Ireland) · Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing3 deaths393 reports
- LCS SIGMA 1294-33-130Depuy (Ireland) · Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing1 recall310 reports
- ATTUNE 1518-20-035Depuy (Ireland) · Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing342 reports
- P.F.C. SIGMA 96-0102Depuy (Ireland) · Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing1 death319 reports
- ATTUNE 1518-20-041Depuy (Ireland) · Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing308 reports
- ATTUNE 1506-10-007Depuy (Ireland) · Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing284 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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