AMF TT CONES 6C21.14.180Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 08033390230919), received between Jul 22, 2026 and Jul 22, 2026 — classified as 1 injury.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJul 22, 2026Adverse Event Without Identified Device or Use Problem

  REVISION SURGERY PERFORMED ON (B)(6) 2026 DUE TO INFECTION. PREVIOUS SURGERY WAS ON (B)(6) 2026 WHEN ANOTHER MANUFACTURER KNEE IMPLANTS USED WITH THE AMF TT CONES: CONE CENTRAL FEMUR D.18 (PN 6C10.14.180, LOT 2401822 STERILIZATION (B)(4)). CONE CENTRAL TIBIA D.18 (PS 6C21.14.180, 2536933 STERILIZATION (B)(4)). AFTER FEW MONTHS PATIENT DEVELOPED AN INFECTION AND THE PRE-EXISTING AMF TT CONES WERE REPLACED WITH NEW ONES WITH DIA 21MM (PN 6C10.14.210 AND 6C21.14.210 RESPECTIVELY). THE WHOLE IMPLANT FROM THE THIRD-PARTY MANUFACTURER WAS ALSO REPLACED. SURGERY WAS COMPLETED AS INTENDED. PATIENT IS MALE, DATE OF BIRTH (B)(6) 1960. THE EVENT OCCURRED IN THE UNITED STATES.

  Patient problems: Medical device site infection

  MAUDE report 25903356 ↗