LCS COMPLETE 1294-12-050Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295022930), received between Oct 24, 2019 and Sep 15, 2021 — classified as 2 injuries.

The most frequently reported specific device problem is “Malposition of Device” (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 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjurySep 15, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED IN THE LEFT KNEE DUE TO ARTHROFIBROSIS. REMOVED FEMUR, INSERT AND TRAY. ORIGINAL DOS IS UNKNOWN. DOI: UNKNOWN, DOR: (B)(6) 2021 , LEFT KNEE.

  Patient problems: Adhesion(s)

  MAUDE report 12473743 ↗
• InjuryOct 24, 2019Malposition of Device; Malposition of Device

  THE PATIENT WAS REVISED TO ADDRESS KNEE PAIN AND LOOSENING OF THE FEMORAL COMPONENT AT THE BONE TO CEMENT INTERFACE. DEPUY CEMENT WAS USED. UPON SURGERY SURGEON DID NOT LIKE ALIGNMENT WHICH WAS POSSIBLY LEADING TO POLY WEAR AND DEEMED FEMUR LOOSE. SURGEON REMOVED COMPONENTS AND REVISED KNEE WITH A TC3. DOI: (B)(6) 2010; DOR: (B)(6) 2019; LEFT KNEE.

  Patient problems: No Code Available; Pain

  MAUDE report 9234854 ↗