LCS COMPLETE 1294-24-420Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295024682), received between Aug 20, 2019 and Jun 30, 2021 — classified as 2 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 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.

• InjuryJun 30, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT UNDERWENT POLY SWAP DUE TO INFECTION. NO LOOSENING REPORTED. DOI: UNKNOWN, DOR: (B)(6) 2021, RIGHT KNEE.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 12093389 ↗
• InjuryAug 20, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED TO ADDRESS FEMORAL PAIN AND SLIGHT INSTABILITY. THE SURGEON REMOVED THE FEMORAL PARTS AND PUT IN A TC3 FEMUR AND INSERT. HE USED A COMPETITOR FEMORAL SLEEVE WITH OUR FEMUR AND STEM IMPLANTS. THE SALES REP ADVISED AGAINST THIS BUT THE SURGEON DECIDED TO DO IT ANYWAY. DOI: (B)(6) 2017; DOR: (B)(6) 2019; RIGHT KNEE.

  Patient problems: No Code Available; Pain

  MAUDE report 8910661 ↗