LCS COMPLETE 1294-29-030Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295025511), received between Feb 12, 2019 and Sep 22, 2020 — classified as 2 injuries.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (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 22, 2020Loss of or Failure to Bond; Adverse Event Without Identified Device or Use Problem; Loss of or Failure to Bond; Adverse Event Without Identified Device or Use Problem

  ADDITIONAL INFORMATION RECEIVED STATED THAT THERE WAS LOOSENING AT THE TIBIAL AND FEMORAL COMPONENTS.

  Patient problems: Inflammation; Limited Mobility Of The Implanted Joint; No Code Available; Pain; Unspecified Infection

  MAUDE report 10567504 ↗
• InjuryFeb 12, 2019Adverse Event Without Identified Device or Use Problem; No Apparent Adverse Event; Adverse Event Without Identified Device or Use Problem; No Apparent Adverse Event

  INTRA-OPERATIVELY, A FEMORAL FRACTURE WAS NOTED AFTER THE KNEE WAS BROUGHT INTO EXTENSION WHILE WAITING FOR FINAL POLYMERIZATION. IT WAS FIXATED WITH A CABLE. DOE: (B)(6) 2014.

  Patient problems: Bone Fracture(s); No Code Available

  MAUDE report 8330822 ↗