LCS COMPLETE 1294-27-041Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295025351), received between Aug 20, 2019 and Aug 20, 2019 — 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 18, 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.

• 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 8910660 ↗
• 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 8910659 ↗