MOTO Partial Knee System - Medial 02.18.TF3.LMRecalls & reported problems
Medacta International SA · Tibial Tray Fix Cemented S3 LM · 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 07630030896736), received between Dec 15, 2017 and Jan 8, 2026 — classified as 6 injuries.
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. 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
- Adverse Event Without Identified Device or Use Problem2
- Appropriate Device Problem Term/Code Not Available2
- Implant subsidence1
- Migration1
Patient problems
- Bone Fracture(s)3
- Pain2
- Implant Pain1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjuryJan 8, 2026Implant subsidence
REVISION SURGERY DUE TO TIBIAL TRAY SUBSIDENCE AT 2 WEEKS FROM PRIMARY. GMK-SPHERE SUCCESSFULLY IMPLANTED.
Patient problems: Implant Pain
MAUDE report 24004368 ↗InjuryDec 9, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION SURGERY DUE TO BONE FRACTURE AT 17 DAYS FROM PRIMARY. THE TIBIAL TRAY HAD COME DOWN TOGETHER WITH THE FRACTURED BONE FRAGMENT. NO TRAUMATIC EVENT REPORTED BY THE PATIENT. THE SURGEON CONVERTED THE PATIENT FROM UNI TO TKA.
Patient problems: Bone Fracture(s)
MAUDE report 23758557 ↗InjuryJun 15, 2022Appropriate Device Problem Term/Code Not Available
REVISION DUE TO TIBIAL BONE FRACTURE 3 WEEKS AFTER PRIMARY. THE SURGEON USED A PLATE AND SCREWS TO FIX THE FRACTURE. FOLLOWING THE FRACTURE REPAIR, THE SURGEON REPLACED THE TIBIAL INSERT.
Patient problems: Bone Fracture(s)
MAUDE report 14696266 ↗InjuryFeb 18, 2022Migration; Migration
THE PATIENT CAME IN REPORTING PAIN DUE TO A SUBSIDED TIBIA AND THE CAUSE IS UNKNOWN. THE SURGEON REVISED ALL IMPLANTS 10 MONTHS AFTER PRIMARY AND THE SURGERY WAS COMPLETED SUCCESSFULLY.
Patient problems: Pain
MAUDE report 13557144 ↗InjuryApr 29, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY PERFORMED AFTER 1 YEAR AND 7 MONTHS FROM THE PRIMARY DUE TO PAIN (THE CAUSE OF PAIN IS UNKNOWN). THE SURGEON REVISED THE MOTO KNEE TO A TOTAL KNEE AND THE SURGERY WAS COMPLETED SUCCESSFULLY.
Patient problems: Pain
MAUDE report 8560453 ↗InjuryDec 15, 2017Adverse Event Without Identified Device or Use Problem
THE PATIENT CAME IN COMPLAINING OF PAIN. THE PATIENT HAD FRACTURED HER TIBIA. THE SURGEON REVISED THE ENTIRE MOTO SYSTEM AND REPLACED IT WITH A TOTAL KNEE. THE SURGERY WAS COMPLETED SUCCESSFULLY. THE BONE FRACTURE CAUSE IS UNKNOWN. THE PATIENT DID NOT REPORT ANY TRAUMA.
Patient problems: Bone Fracture(s)
MAUDE report 7120563 ↗
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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