MOTO Partial Knee System 02.18.702RMRecalls & reported problems
Medacta International SA · TiNbN coated Anatomical Femur Cemented S2 RM - MEDIAL · Class 2 · Implant
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07630345705228), received between Nov 10, 2025 and Nov 10, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Implant subsidence” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Implant subsidence1
- Loosening of Implant Not Related to Bone-Ingrowth1
- Malposition of Device1
Patient problems
- Aseptic loosening1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 10, 2025Malposition of Device; Loosening of Implant Not Related to Bone-Ingrowth; Implant subsidence; Malposition of Device; Loosening of Implant Not Related to Bone-Ingrowth; Implant subsidence
AT ABOUT 2 WEEKS AFTER THE PRIMARY, THE PATIENTCAME IN REPORTING PAIN DUE TO A LOOSE AND SUBSIDED BASEPLATE AND THE CAUSE IS UNKNOWN. THE PATIENT DIDN & RSQUO; T COMPLAIN ANY FALLS BUT MENTIONED POSSIBLY OVERDOING ACTIVITY, FEELING WELL FOR THE FIRST TIME IN YEARS. THE SURGEON FOUND THE BASEPLATE/POLYETHYLENE GROSSLY LOOSE AND SUSPECTED A CEMENT ISSUE, AS THE INITIAL FIT HAD BEEN EXCELLENT. THE SURGEON REVISED ALL COMPONENTS. THE SURGERY WAS COMPLETED SUCCESSFULLY. ADDITIONAL NOTE FOR CLINICAL INTERNAL ANALYSES: THE X-RAY SHOWS THAT THE FEMORAL COMPONENT APPEARS TO BE POSITIONED IN FLEXION, WITH AN IMPERFECT FIT TO THE FEMORAL BONE; THEREFORETHE LEVEL 2 CHANGE THE CLASSIFICATION FROM ASSOCIATED COMPONENT TO MALPOSITIONING.
Patient problems: Aseptic loosening
MAUDE report 23510665 ↗
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
- Arthrex® AR-503-TTTGArthrex, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER1 recall7 reports
- ENGAGE 1-10011-300Smith & Nephew, 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.