LCS COMPLETE 1294-09-860Recalls & reported problems

Summary

The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 10603295022800), received between May 9, 2019 and Jun 15, 2026 — classified as 9 injuries.

The most frequently reported specific device problem is “Naturally Worn” (3 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 18, 2026.

Most reported problems

Recent adverse event reports

The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.

• InjuryJun 15, 2026Naturally Worn

  IT WAS REPORTED THAT PATELLA POLY WEAR. TIBIAL INSERT WEAR. AFFECTED SIDE: RIGHT KNEE.

  Patient problems: Insufficient Information

  MAUDE report 25505574 ↗
• InjuryApr 21, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT HAD A WOUND DEHISCENCE FOLLOWING A PATELLAR SWAP AND I&D A MONTH PRIOR. SURGEON DECIDED TO OPEN THE JOINT AND WASH OUT WHILE REVISING THE WOUND. POLY AND PATELLA POLY WERE REPLACED DURING THE WASH OUT. AFFECTED SIDE: LEFT KNEE.

  Patient problems: Wound Dehiscence

  MAUDE report 21878013 ↗
• InjuryMar 21, 2025Naturally Worn; Naturally Worn

  IT WAS REPORTED THAT PATELLA BUTTON HAD WEAR AND WAS REPLACED ALONG WITH AN I&D OF THE LEFT KNEE. THERE WAS NO SURGICAL DELAY; NO PATIENT CONSEQUENCE. DOI: UNKNOWN. DOR: (B)(6) 2025. AFFECTED SIDE: LEFT KNEE.

  Patient problems: Insufficient Information

  MAUDE report 21666581 ↗
• InjuryOct 14, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PATIENT WAS REVISED DUE TO PAINFUL RIGHT KNEE. THERE WAS NO SURGICAL DELAY. DOI: (B)(6) 2016. DOR: (B)(6) 2022. AFFECTED SIDE: RIGHT KNEE.

  Patient problems: Pain

  MAUDE report 15604967 ↗
• InjuryNov 8, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT'S KNEE WAS REVISED DUE TO PAIN. DOI: UNK. DOR: (B)(6) 2021. RIGHT KNEE.

  Patient problems: Pain

  MAUDE report 12770942 ↗
• InjuryJan 22, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED TO ADDRESS MCL DEFICIENT. ORIGINAL IMPLANT DATE UNKNOWN. NO SURGICAL DELAY. DOI: UNKNOWN; DOR: (B)(6) 2021; LEFT KNEE.

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

  MAUDE report 11212903 ↗
• InjuryJul 14, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE PATIENT WAS REVISED DUE TO PAIN. DOI: (B)(6) 2000, DOR: (B)(6) 2020, RIGHT KNEE.

  Patient problems: No Code Available; Pain

  MAUDE report 10270956 ↗
• InjuryMay 20, 2019Fracture; Fracture

  IT WAS REPORTED THAT PATIENT HAD A LCS COMPLETE PRESSFIT KNEE DONE APPROXIMATELY 10 YEARS AGO. PATIENT FELL IN DECEMBER AND FRACTURED THE POLY OF THE METAL BACKED PATELLA. THE PATELLA WAS REVISED AND A NEW POLY PATELLA WAS ATTACHED TO THE RETAINED METAL BACKED PATELLA BASE. THE PRESSFIT FEMUR AND TIBIA WERE WELL FIXED AND RETAINED AS WELL AS THE POLY TIBIAL INSERT. DOI: 10 YEARS AGO; DOR: (B)(6) 2019, LEFT KNEE.

  Patient problems: No Code Available

  MAUDE report 8623414 ↗
• InjuryMay 9, 2019Naturally Worn; Naturally Worn

  IT WAS REPORTED THAT THE POLY WAS REPLACED. THE WORN POLY WAS LEADING TO PAIN. DOI: UNKNOWN. DOR: (B)(6) 2019. LEFT KNEE.

  Patient problems: No Code Available; Pain

  MAUDE report 8596645 ↗