Trident 621-10-36GRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327023725), received between May 4, 2022 and May 4, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Degraded” (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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryMay 4, 2022Degraded; Degraded

  IT WAS REPORTED THROUGH THE FILING OF A LAWSUIT THAT ALLEGEDLY THE PATIENT WAS IMPLANTED WITH AN LFIT ANATOMIC COCR V40 FEMORAL HEAD ON HIS RIGHT HIP ON OR ABOUT (B)(6) 2014 AND WAS REVISED ON (B)(6) 2020. IT IS FURTHER ALLEGED THAT HE SUFFERED INJURIES AS A RESULT OF IMPLANTATION AND EXPLANTATION OF THE DEVICE(S) AT ISSUE, DEVICE RECALL AND EXCESSIVE LEVELS OF CHROMIUM AND COBALT IN HIS BLOOD. UPDATE AS PER MEDICAL REVIEW (B)(6) 2022. INTRAOPERATIVE FINDINGS INCLUDED "BLACK FLUID CORROSION AT TRUNNION AND FEMORAL HEAD INNER SURFACE, HEALTHY APPEARING MUSCLE, WELL FIXED COMPONENTS, SIGNIFICANT WEAR IN THE POSTERIOR SUPERIOR RIM OF THE ACETABULAR POLYETHYLENE.

  Patient problems: Discomfort; Metal Related Pathology

  MAUDE report 14276090 ↗