LCS COMPLETE 1294-29-040Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295025528), received between Feb 7, 2019 and Mar 15, 2022 — classified as 4 injuries.

The most frequently reported specific device problem is “Loss of or Failure to Bond” (2 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 16, 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.

• InjuryMar 15, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  REVISION OF LCS REVISION BECAUSE OF PAIN AND STIFFNESS - REVISED TO A HINGE FROM ANOTHER COMPANY. DOI: (B)(6) 2019. DOR: (B)(6) 2022. UNKNOWN SIDE.

  Patient problems: Muscular Rigidity; Pain

  MAUDE report 13769526 ↗
• InjuryOct 22, 2019Loss of or Failure to Bond; Device Dislodged or Dislocated; Loss of or Failure to Bond; Device Dislodged or Dislocated

  HEIGHT: 157. OPERATED SIDE: LEFT.

  Patient problems: No Code Available

  MAUDE report 9221164 ↗
• InjuryMar 29, 2019Loss of or Failure to Bond; Loss of or Failure to Bond

  PATIENT HAD A REVISION KNEE FOR ONGOING PAIN. MRI SHOWED AN INCREASED UPTAKE AROUND THE FEMUR-THIS WAS STATED IN THE NOTES AND CAN INDICATE LOOSENING OF THE COMPONENT.

  Patient problems: No Code Available; Pain

  MAUDE report 8463842 ↗
• InjuryFeb 7, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE EVENT STATED THAT THE PATIENT HAD A PAINFUL KNEE AND WAS REVISED.

  Patient problems: No Code Available; Pain

  MAUDE report 8314608 ↗