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

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07630030896729), received between Feb 26, 2019 and Oct 25, 2023 — classified as 5 injuries.

The most frequently reported specific device problem is “Fracture” (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

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryOct 25, 2023Migration or Expulsion of Device; Migration or Expulsion of Device

  REVISION SURGERY WAS PERFORMED AT ABOUT 2 MONTHS AFTER THE PRIMARY DUE TO CEMENTED TIBIAL TRAY SUBSIDENCE. MOTO COMPONENTS HAVE BEEN SUCCESSFULLY REVISED. THE PATIENT HAS POOR BONE QUALITY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18002681 ↗
• InjuryJan 25, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  A PRIMARY KNEE SURGERY WAS PERFORMED ON THE (B)(6) 2022. AT ABOUT 2 WEEKS AFTER THE PRIMARY SURGERY, A TIBIA BONE FRACTURE WAS DETECTED. THE CAUSE OF THE FRACTURE IS UNKNOWN. PRESENTLY ON THE (B)(6) 2022, A REVISION SURGERY WAS PERFORMED AND THE FRACTURE WAS SUCCESSFULLY FIXED WITH LCP PLATE.

  Patient problems: Bone Fracture(s)

  MAUDE report 16240560 ↗
• InjurySep 8, 2021Output Problem

  3 MONTHS AFTER THE PRIMARY SURGERY A REVISION WAS PERFORMED DUE TO THE SINKING OF THE MEDIAL TIBIAL PLATEAU. THE PATIENT REPORTED THAT SHE HAD NOT FALLEN. THE SURGEON REVISED ALL IMPLANTS.

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

  MAUDE report 12438439 ↗
• InjuryJun 17, 2020Fracture; Appropriate Device Problem Term/Code Not Available

  SUBSIDENCE OF THE TIBIAL TRAY, DUE TO POST-OP FRACTURE (THE ROOT CAUSE OF THE BONE FRACTURE IS UNKNOWN) OF THE MEDIAL TIBIAL HEAD. 4 MONTHS AFTER PRIMARY THE SURGEON REVISED ALL IMPLANTS TO GMK SPHERE.

  Patient problems: Bone Fracture(s)

  MAUDE report 10161544 ↗
• InjuryFeb 26, 2019Loosening of Implant Not Related to Bone-Ingrowth

  REVISION SURGERY PERFORMED DUE TO A LOOSENING OF THE TIBIAL TRAY CAUSED BY A BONE FRACTURE CLOSE TO THE ANTERIOR FIXATION PEG. AFTER A FEW WEEKS FROM THE UNICOMPARTMENTAL KNEE REPLACEMENT SURGERY, PERFORMED WITH A MOTO IMPLANT ON (B)(6) 2018, DESPITE POST-OP X-RAYS WERE GOOD, THE PATIENT CAME BACK TO THE SURGEON COMPLAINING ABOUT MILD MEDIAL KNEE PAIN. AFTER A FURTHER CLINICAL INVESTIGATION, THE SURGEON OBSERVED A BONE FRACTURE OF THE TIBIAL PLATE CLOSE TO THE ANTERIOR FIXATION PEG. AFTER MONITORING PERIOD OF THE CASE, ON (B)(6) 2019, THE SURGEON DECIDED TO REOPERATE THE PATIENT, ALL COMPONENTS WERE REMOVED.

  Patient problems: Bone Fracture(s)

  MAUDE report 8370496 ↗