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MOTO Partial Knee System - Medial 02.18.TF3.RMRecalls & reported problems

Medacta International SA · Tibial Tray Fix Cemented S3 RM · 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
6
Deaths reported
0
Injuries reported
6
Recalls naming it
0

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 07630030896743), received between Sep 29, 2017 and Jun 4, 2025 — classified as 6 injuries.

The most frequently reported specific device problem is “Fracture” (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 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: 1 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 1 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 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

  • Fracture2
  • Adverse Event Without Identified Device or Use Problem1
  • Appropriate Device Problem Term/Code Not Available1
  • Implant subsidence1
  • Loose or Intermittent Connection1

Patient problems

  • Bone Fracture(s)3
  • Implant Pain1
  • Insufficient Information1
  • Joint Disorder1
  • Pain1

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

  • InjuryJun 4, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IN THE POST OP X-RAYS A LITTLE FRACTURE WAS VISIBLE WHERE THE PIN WAS INSERTED FOR CUTTING GUIDE FIXATION. AT 2 MONTHS POST PRIMARY A TIBIAL BONE DEFORMATION IS VISIBLE. IT IS DUE TO THE BONE DEPRESSION AT LEVEL OF THE FRACTURE GENERATED BY THE PIN. NO MORE INFO IS AVAILABLE. NO REVISION SURGERY REPORTED DUE TO THIS EVENT.

    Patient problems: Bone Fracture(s)

    MAUDE report 22141038 ↗
  • InjuryDec 30, 2024Implant subsidence; Implant subsidence

    AT ABOUT 6 YEARS AND 1 MONTHS AFTER PRIMARY, THE PATIENT CAME IN REPORTING PAIN DUE TO A SUBSIDED TIBIAL COMPONENT. THE CAUSE OF THE SUBSIDED TIBIAL COMPONENT IS UNKNOWN. THE SURGEON REVISED ALL COMPONENTS FROM MOTO TO GMK-SPHERE AND THE SURGERY WAS COMPLETED SUCCESSFULLY.

    Patient problems: Implant Pain

    MAUDE report 21033492 ↗
  • InjuryNov 26, 2021Fracture

    DURING THE PRIMARY KNEE SURGERY, WHEN THE SURGEON WAS IMPACTING THE TIBIAL BASEPLATE FINAL IMPLANT, THE SURGEON OBSERVED A TIBIAL PLATEAU FRACTURE. IT IS UNKNOWN HOW THE FRACTURE OCCURRED. THE SURGEON PUT A PLATE ON THE ANTERIOR ASPECT OF THE TIBIA AND THE SURGERY WAS COMPLETED SUCCESSFULLY. THERE WAS A 15-MINUTE DELAY AND A CONSIGNMENT SET WAS UTILIZED.

    Patient problems: Bone Fracture(s)

    MAUDE report 12878077 ↗
  • InjuryNov 24, 2021Appropriate Device Problem Term/Code Not Available

    AT 1 YEAR 5 MONTHS AFTER THE PRIMARY THE PATIENT CAME IN REPORTING FLEXION INSTABILITY AND THE CAUSE IS UNKNOWN. THE SURGEON REVISED THE PATIENT TO A TOTAL KNEE AND THE SURGERY WAS COMPLETED SUCCESSFULLY.

    Patient problems: Insufficient Information

    MAUDE report 12867456 ↗
  • InjuryOct 4, 2018Loose or Intermittent Connection

    REVISION DUE TO LOOSENING OF THE TIBIAL TRAY 2 MONTHS AFTER THE PRIMARY, DUE TO A WEAKENING OF THE UNDERLYING BONE STOCK. THE SURGEON REVISED ALL THE DEVICES.

    Patient problems: Joint Disorder

    MAUDE report 7933739 ↗
  • InjurySep 29, 2017Fracture

    THE PATIENT CAME IN COMPLAINING OF PAIN. THE PATIENT ALSO HAD A FATIGUE FRACTURE OF THE TIBIAL BONE. THE SURGEON REVISED ALL MEDACTA HARDWARE. THE SURGERY WAS COMPLETED SUCCESSFULLY.

    Patient problems: Bone Fracture(s); Pain

    MAUDE report 6903984 ↗

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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