LCS 1278-24-000Recalls & reported problems
Depuy Orthopaedics, Inc. · LCS TIBIAL INSERT MENISCAL BEARING BRIDGING BEARING STD+/LG 10mm · Class 3 · Implant
All models of LCS (45)
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 10603295020394), received between Aug 21, 2018 and Jul 15, 2025 — classified as 4 injuries.
The most frequently reported specific device problem is “Naturally Worn” (4 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 Worn4
Patient problems
- Insufficient Information2
- No Code Available1
- No Consequences Or Impact To Patient1
- Not Applicable1
- Pain1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryJul 15, 2025Naturally Worn; Naturally Worn
IT WAS REPORTED THAT THE PATIENT UNDERWENT REVISION SURGERY DUE TO POLY WEAR.
Patient problems: Insufficient Information
MAUDE report 22505451 ↗InjuryOct 18, 2022Naturally Worn; Naturally Worn
REVISION COMPLETED DUE TO POLY WEAR.
Patient problems: Insufficient Information
MAUDE report 15626295 ↗InjuryJul 3, 2019Naturally Worn; Naturally Worn
AFFECTED SIDE IS THE LEFT KNEE. THE PATIENT SUFFERED 3 TO 4 YEARS OF INTERMITTENT PAIN.
Patient problems: No Code Available; No Consequences Or Impact To Patient; Pain
MAUDE report 8757505 ↗InjuryAug 21, 2018Naturally Worn; Naturally Worn
POLY WEAR. PATIENT CONSEQUENCE? :YES. PATIENT CONSEQUENCE DESCRIPTION:POLY CHANGE. ACTION TAKEN FOR PROCEDURE:ACTION FOR NEW POLY. IS THE INFORMATION BEING SUBMITTED FOR THIS COMPLAINT ALL THE DETAILS THAT ARE KNOWN/AVAILABLE REGARDING THIS EVENT? : YES.
Patient problems: Not Applicable
MAUDE report 7800930 ↗
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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