MOTO Partial Knee System 02.18.EIF4.08.RMRecalls & reported problems
Medacta International SA · E-CROSS tibial insert fix S4 RM - 8mm · Class 2 · Implant
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07630345711694), received between Apr 23, 2026 and Aug 11, 2026 — classified as 3 injuries.
The most frequently reported specific device problem is “Device Appears to Trigger Rejection” (3 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Device Appears to Trigger Rejection3
Patient problems
- Medical device site infection3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryAug 11, 2026Device Appears to Trigger Rejection
At about 1 months from the primary, the patient came in due to infection and the pathogen is unknown. The surgeon performed a washout and revised the MOTO Medial E-CROSS tibial insert S4 RM - H8 to a same size insert. The surgery was completed successfully.
Patient problems: Medical device site infection
MAUDE report 50209586 ↗InjuryAug 3, 2026Device Appears to Trigger Rejection
Revision surgery due to infection after about 1 month from primary.The surgeon performed a washout and revised the poly.
Patient problems: Medical device site infection
MAUDE report 50114134 ↗InjuryApr 23, 2026Device Appears to Trigger Rejection
AT ABOUT 6 MONTHS FROM THE PRIMARY, THE PATIENT CAME IN DUE TO SIGNS OF AN INFECTION AND THE PATHOGEN IS UNKNOWN. THE SURGEON PERFORMED A WASHOUT AND REVISED THE S4 - H8 MOTO INSERT TO A SAME SIZE INSERT. THE SURGERY WAS COMPLETED SUCCESSFULLY.
Patient problems: Medical device site infection
MAUDE report 24964776 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.