LCS 1178-24-025Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295007807), received between Oct 16, 2020 and Feb 6, 2026 — classified as 4 injuries.

The most frequently reported specific device problem is “Naturally Worn” (3 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.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 6, 2026Naturally Worn

  ADDITIONAL INFORMATION RECEIVED STATES THAT THE AFFECTED SIDE INVOLVED IN THIS EVENT IS THE RIGHT KNEE.

  Patient problems: Joint Laxity; Pain

  MAUDE report 24277888 ↗
• InjurySep 30, 2024Naturally Worn; Naturally Worn

  REVISION OF AN LCS MENISCAL BEARING IN PATIENT X NECESSARY DUE TO WEAR OF THE INSERT. REVISION IS NOT PLANNED YET.

  Patient problems: Insufficient Information

  MAUDE report 20332605 ↗
• InjuryJan 19, 2024Naturally Worn; Adverse Event Without Identified Device or Use Problem; Naturally Worn; Adverse Event Without Identified Device or Use Problem

  ADDITIONAL INFORMATION RECEIVED. IT¿S FOR INSTABILITY, DUE TO SUSPECTED INSERT POLY WEAR.

  Patient problems: Insufficient Information; Joint Laxity

  MAUDE report 18544228 ↗
• 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 10692120 ↗