LCS COMPLETE 1294-05-210Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295021872), received between Dec 14, 2021 and Dec 14, 2021 — classified as 1 injury.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryDec 14, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT REPORTED PATELLAR INSTABILITY SINCE ABOUT ONE YEAR WITH EVENTUAL KNEE INSTABILITY IN GENERAL. PAIN BECAME IMMOBILIZING AND PATIENT REPORTED TO PARTNER HOSPITAL (B)(6) AT THE EMERGENCY DEPARTMENT. A SUBLUXATED KNEE PROSTHESIS WAS DIAGNOSED AND REPONATED, THEREAFTER PATIENT WAS REFERRED TO (B)(6). PATIENT REPORTED TO (B)(6) AND WAS WEARING A KNEE BRACE FOR STABILITY. INTRAOPERATIVE KNEE INSTABILITY WAS OBSERVED TOGETHER WITH DISSOCIATING PATELLAR INLAY, WHICH MAY BE EXPLAINED BY REPEATED PATELLAR SUBLUXATIONS AND RESULTING EXCENTRIC LOADS. DOI: UNKNOWN, DOR: (B)(6) 2021, UNKNOWN SIDE.

  Patient problems: Joint Laxity; Pain

  MAUDE report 13001337 ↗