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
- LinkSymphoKnee 880-307/21WALDEMAR LINK GmbH & Co. KG · PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER2 recalls2 reports
- Scorpio 73-3710Howmedica Osteonics Corp. · PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER2 recalls1 report
- Scorpio 73-3110Howmedica Osteonics Corp. · PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER2 recalls0 reports
- Arthrex® AR-503-TTTEArthrex, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall14 reports
- Arthrex® AR-503-TTTJArthrex, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall9 reports
- ENGAGE 1-10011-300Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall7 reports
- Arthrex® AR-503-TTTGArthrex, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall7 reports
- ENGAGE 1-10003-400Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall6 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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