LCS COMPLETE 1294-05-420Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295022053), received between Aug 15, 2017 and Aug 21, 2019 — classified as 3 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 18, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryAug 21, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE DOCTOR SAID THE PATIENT HAD PAIN FOLLOWING A PREVIOUS POLY EXCHANGE DONE YEARS AGO. HE PERFORMED SOME SOFT TISSUE RELEASES TO HELP BALANCE THE PATIENT'S KNEE AND EXCHANGED BOTH THE TIBIAL INSERT AND METAL BACKED PATELLA POLY. DOI: (B)(6) 2014; DPR: (B)(6) 2019, LEFT KNEE.

  Patient problems: No Code Available; Pain

  MAUDE report 8915527 ↗
• InjuryDec 7, 2018Unstable; Appropriate Device Problem Term/Code Not Available; Unstable; Appropriate Device Problem Term/Code Not Available

  PATIENT WAS REVISED TO ADDRESS PAIN AND INSTABILITY.

  Patient problems: Pain

  MAUDE report 8142095 ↗
• InjuryAug 15, 2017Insufficient Device Problem Information; Insufficient Device Problem Information

  THE PATIENT WAS REVISED TO ADDRESS PAIN IN THE RIGHT KNEE.

  Patient problems: Pain

  MAUDE report 6793766 ↗