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
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
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page