LCS 1180-27-000Recalls & reported problems
Depuy Orthopaedics, Inc. · LCS TIBIAL TRAY MENISCAL BEARING POST CRUCIATE RETAINING STD+ CEMENTED · Class 3 · Implant
All models of LCS (45)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295008309), received between Oct 2, 2017 and Oct 16, 2020 — classified as 2 injuries.
The most frequently reported specific device problem is “Loss of Osseointegration” (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
- Adverse Event Without Identified Device or Use Problem1
- Loss of Osseointegration1
Patient problems
- Pain2
- No Code Available1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryOct 16, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
EVENT DESCRIPTION OF COMPLAINT (PLEASE SUPPLY SPECIFIC DETAILS): PLANNED REVISION OF LCS KNEE OPERATED IN 2003 DUE TO STIFFNESS AND PAIN. PATIENT WAS REVISED TO A LCS VVC REVISION KNEE WITH NO ADVERSE EVENTS. IMPLANTS WILL NOT BE RETURNED. DOI: 2003; DOR: (B)(6) 2020; UNKNOWN SIDE.
Patient problems: No Code Available; Pain
MAUDE report 10692106 ↗InjuryOct 2, 2017Loss of Osseointegration; Loss of Osseointegration
THE PATIENT WAS REVISED TO ADDRESS PAIN AND LOOSENING OF THE TIBIAL TRAY AT UNKNOWN INTERFACE. UPDATE 9/4/2017: DETERMINED THAT THE TIBIAL BASEPLATE COMPONENT IS A PRESS-FIT, POROUS COATED COMPONENT, WITH REGARD TO LOOSENING INTERFACE (BONE TO IMPLANT). COMPLAINT UPDATED ON: 10/2/2017.
Patient problems: Pain
MAUDE report 6907404 ↗
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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