MOTO Partial Knee System - Medial 02.18.TF2.LMRecalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 07630030896712), received between Aug 11, 2020 and Feb 16, 2026 — classified as 6 injuries.

The most frequently reported specific device problem is “Migration” (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.

Most reported problems

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjuryFeb 16, 2026Loosening of Implant Not Related to Bone-Ingrowth

  AT ABOUT 2 MONTHS AFTER THE PRIMARY, THE PATIENT REPORTED PAIN ASSOCIATED WITH TIBIAL COMPONENT LOOSENING. RADIOGRAPHIC EVALUATION REVEALED A FRACTURE OF THE TIBIAL MEDIAL COMPARTMENT. PATIENT`S BONE QUALITY NORMAL. IT IS LIKELY THAT THE FRACTURE WORSENED DUE TO THE PATIENT WALKING ON THE ALREADY FRACTURED TIBIA WHILE MANAGING PAIN WITH MEDICATION. THE SURGEON CONVERTED THE PARTIAL KNEE ARTHROPLASTY TO A TOTAL KNEE ARTHROPLASTY, AND THE REVISION SURGERY WAS COMPLETED SUCCESSFULLY.

  Patient problems: Aseptic loosening; Bone Fracture(s)

  MAUDE report 24343902 ↗
• InjuryJun 25, 2025Adverse Event Without Identified Device or Use Problem; Migration; Adverse Event Without Identified Device or Use Problem; Migration

  REVISION SURGERY AT ABOUT 9 DAYS FROM PRIMARY DUE TO A SUBSIDED TIBIAL COMPONENT. THE CAUSE OF THE SUBSIDED TIBIAL COMPONENT IS UNKNOWN. THE SURGEON REVISED ALL MOTO COMPONENTS TO SPHERIKA COMPONENTS. THE SURGERY WAS COMPLETED SUCCESSFULLY.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 22326809 ↗
• InjuryJan 8, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  AT ABOUT 2 MONTHS AFTER PRIMARY, REVISION HAS BEEN PERFORMED DUE TO TIBIAL BONE FRACTURE, THE CAUSE IS UNKNOWN. IT IS NOT POSSIBLE TO DEFINE IF THE FRACTURE MAY BE DUE TO TRAUMATIC EVENT OR TO THE PROGRESSIVE DESTABILIZATION OF BONE. MOTO COMPONENTS HAVE BEEN REVISED SUCCESSFULLY AND THE SURGEON IMPLANTED GMK SPHERE FEMUR AND INSERT AND GMK REVISION TIBIA WITH HIGH WEDGES AND STEM.

  Patient problems: Bone Fracture(s)

  MAUDE report 21102487 ↗
• InjuryMar 21, 2024Migration; Migration

  REVISION SURGERY FOR TIBIAL TRAY SUBSIDENCE, NO ADDITIONAL INFO AVAILABLE.

  Patient problems: Insufficient Information

  MAUDE report 18950298 ↗
• InjuryJun 22, 2022Adverse Event Without Identified Device or Use Problem

  DURING THE PRIMARY KNEE SURGERY, AFTER THE MOTO FEMUR, INSERT AND TIBIA WERE IMPLANTED THE SURGEON PERFORMED A RANGE OF MOTION CONTROL AND AN EXCESSIVE TIBIAL BASEPLATE MOVEMENT, ALONG THE X-AXIS, WAS OBSERVED. DUE TO THIS, THE SURGEON DECIDED TO CONVERT THE UKA TO TKA, PROBABLY DUE TO THE FACT THAT HE MAY HAVE FELT THE TIBIAL PREPARATION LED TO THE TIBIA TOO MEDIAL AND STRUCTURALLY COMPROMISED AND UNABLE TO SUPPORT UKA. THIS DECISION, TO CONVERT TO TKA, EXTENDED THE CASE ROUGHLY 20-25 MINUTES.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 14776852 ↗
• InjuryAug 11, 2020Appropriate Device Problem Term/Code Not Available

  THE PATIENT CAME IN REPORTING PAIN AND THE CAUSE OF THE PAIN IS UNKNOWN. THE SURGEON REPLACED THE UNI IMPLANTS AND IMPLANTED A TKA 2 YEARS AND 11 MONTHS AFTER PRIMARY. THE SURGERY WAS COMPLETED SUCCESSFULLY.

  Patient problems: Pain

  MAUDE report 10389664 ↗