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MOTO Partial Knee System - Medial 02.18.IF4.09.LMRecalls & reported problems

Medacta International SA · Tibial insert fix S4 LM - 9mm · Class 2 · Implant

All models of MOTO Partial Knee System - Medial (46)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
4
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07630030896118), received between Dec 27, 2017 and Oct 31, 2025 — classified as 2 injuries, 2 malfunctions.

The most frequently reported specific device problem is “Device Issue” (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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 1 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem3
  • Device Issue1

Patient problems

  • Unspecified Infection2
  • No Clinical Signs, Symptoms or Conditions1
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

  • MalfunctionOct 31, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    THE SURGEON ATTEMPTED TO INSERT THE LINER INTO THE TIBIAL TRAY, BUT IT DIDN'T LOCK SECURELY. A SECOND INSERT WAS USED; HOWEVER, IT ALSO FAILED TO LOCK PROPERLY. THE CAUSE OF THESE ISSUES REMAINS UNKNOWN. FINALLY, AN 8MM INSERT WAS SUCCESSFULLY FIXED, AND THE SURGERY WAS COMPLETED WITHOUT FURTHER COMPLICATIONS. THE TOTAL SURGERY TIME WAS 2 HOURS, INCLUDING A 40-MINUTE DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23437070 ↗
  • InjuryFeb 3, 2022Adverse Event Without Identified Device or Use Problem

    THE PATIENT CAME IN DUE TO SIGNS OF AN INFECTION AND THE PATHOGEN IS UNKNOWN. ABOUT 1 MONTH AFTER THE PRIMARY SURGERY, THE SURGEON PERFORMED A WASHOUT AND REVISED THE POLY AND THE SURGERY WAS COMPLETED SUCCESSFULLY.

    Patient problems: Unspecified Infection

    MAUDE report 13440332 ↗
  • InjuryJul 2, 2021Adverse Event Without Identified Device or Use Problem

    1 MONTH AFTER THE PRIMARY SURGERY THE PATIENT CAME IN DUE TO SIGNS OF AN INFECTION AND THE PATHOGEN IS UNKNOWN. THE SURGEON PERFORMED A WASHOUT AND REVISED THE POLY AND THE SURGERY WAS COMPLETED SUCCESSFULLY.

    Patient problems: Unspecified Infection

    MAUDE report 12106294 ↗
  • MalfunctionDec 27, 2017Device Issue; Device Issue

    DURING A MOTO PRIMARY CASE, THE IMPLANT WOULDN'T LOCK INTO THE BASEPLATE EVEN IF THE SURGEON TRIED FOR SEVERAL TIMES. HE THEN PUT INA TRIAL INSERT TO ALLOW THE CEMENT TO CURE AND THEN OPENED A SECONDARY IMPLANT TO COMPLETE THE SURGERY. 2 MINUTE OF DELAY. THE SURGERY WAS COMPLETED SUCCESSFULLY.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7147253 ↗

Other Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer devices

All Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer devices →

Sources and updates

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