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MOTO Partial Knee System - Medial 02.18.IF5.08.RMRecalls & reported problems

Medacta International SA · Tibial insert fix S5 RM - 8mm · 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
4
Recalls naming it
0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07630030896224), received between May 3, 2019 and Nov 20, 2020 — classified as 4 injuries.

The most frequently reported specific device problem is “Positioning Failure” (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

Device problems

  • Appropriate Device Problem Term/Code Not Available3
  • Positioning Failure1

Patient problems

  • Unspecified Infection2
  • Insufficient Information1
  • Pain1

Recent adverse event reports

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

  • InjuryNov 20, 2020Positioning Failure

    DURING THE PRIMARY KNEE SURGERY, WHEN THE SURGEON WENT TO SNAP THE TIBIAL INSERT FIX S5 RM - 8MM INTO PLACE, IT WOULD NOT LOCKDOWN. THE AGENT RETRIEVED A NEW 8 MM TIBIAL INSERT, WHICH ALSO DID NOT LOCK IN OR SEAT. THE SURGEON IMPLANTED THE 2ND INSERT INTO THE PATIENT, HOWEVER, IT NEVER LOCKED INTO PLACE. A THIRD 8 MM LINER WAS NOT AVAILABLE IN THE SET. BONE AND SOFT TISSUE WERE DEBRIEFED AWAY AND NOT INTERFERING WITH THE LOCKING MECHANISM. THE TIBIAL RAILS WERE CLEAR AND THE SURGEON CHECKED FOR BONE AND CEMENT WITH NONE TO BE FOUND.

    Patient problems: Insufficient Information

    MAUDE report 10875419 ↗
  • InjuryJun 5, 2020Appropriate Device Problem Term/Code Not Available

    THE PATIENT CAME IN REPORTING PAIN AND THE CAUSE IS UNKNOWN. 6 MONTHS AFTER PRIMARY THE SURGEON REVISED ALL IMPLANTS AND CONVERTED THE PATIENT FROM A PARTIAL KNEE TO A TOTAL KNEE SYSTEM. THE SURGERY WAS COMPLETED SUCCESSFULLY.

    Patient problems: Pain

    MAUDE report 10122100 ↗
  • InjuryFeb 11, 2020Appropriate Device Problem Term/Code Not Available

    THE PATIENT CAME IN, 2 MONTHS AFTER PRIMARY SURGERY, DUE TO SIGNS OF AN INFECTION AND THE PATHOGEN IS UNKNOWN. THE SURGEON PERFORMED A WASHOUT AND POLY-SWAP AND THE SURGERY WAS COMPLETED SUCCESSFULLY.

    Patient problems: Unspecified Infection

    MAUDE report 9693400 ↗
  • InjuryMay 3, 2019Appropriate Device Problem Term/Code Not Available

    THE PATIENT CAME IN, LESS THAN ONE MONTH AFTER PRIMARY SURGERY, DUE TO SIGNS OF INFECTION AND THE PATHOGEN IS UNKNOWN. THE SURGEON PERFORMED AN I&D AND POLY SWAP AND THE SURGERY WAS COMPLETED SUCCESSFULLY.

    Patient problems: Unspecified Infection

    MAUDE report 8577876 ↗

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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