LCS COMPLETE 1294-09-560Recalls & reported problems
Depuy (Ireland) · LCS COMPLETE All Poly Patella LRG · Class 3 · Implant
All models of LCS COMPLETE (18)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10603295022596), received between Apr 7, 2020 and Feb 9, 2026 — classified as 5 injuries.
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
- Adverse Event Without Identified Device or Use Problem5
- No Apparent Adverse Event1
Patient problems
- No Code Available2
- Unspecified Infection2
- Joint Contracture1
- Joint Laxity1
- Loss of Range of Motion1
- Muscular Rigidity1
- Pain1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryFeb 9, 2026Adverse Event Without Identified Device or Use Problem; No Apparent Adverse Event
REVISION OF LCS BEARING DUE TO INSTABILITY. THE BEARING THICKNESS NEEDED TO BE THICKER TO INCREASE STABILITY. BEARING WAS UPSIZED FROM 10MM TO 15MM. NO OTHER COMPONENTS WERE REVISED.
Patient problems: Joint Laxity
MAUDE report 24292030 ↗InjuryMay 20, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE KNEE HAD A 40 DEGREE CONTRACTURE AND WAS TIGHT. NO SURGICAL DELAY. DOI: (B)(6). DOR: (B)(6). LEFT KNEE.
Patient problems: Joint Contracture; Loss of Range of Motion; Muscular Rigidity
MAUDE report 11858281 ↗InjuryApr 28, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE PATIENT HAD PAIN FOLLOWING A CYST THAT FORMED ON THE LATERAL FEMORAL CONDYLE. THIS NECESSITATED THE REMOVAL OF THE PROSTHESIS.
Patient problems: Pain
MAUDE report 11738127 ↗InjurySep 16, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT IS INFECTED. EXPLANTED COMPONENTS AND PUTTING IN STATIC SPACER WAS DONE. DOI: (B)(6) 2020. DOR: (B)(6) 2020. RIGHT KNEE.
Patient problems: No Code Available; Unspecified Infection
MAUDE report 10540196 ↗InjuryApr 7, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE PATIENT WAS REVISED TO ADDRESS INFECTION. DOI: UNKNOWN; DOE: (B)(6) 2020; LEFT KNEE.
Patient problems: No Code Available; Unspecified Infection
MAUDE report 9933340 ↗
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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