LFIT 06-3605Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327072358), received between Jun 18, 2018 and Mar 22, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Corroded” (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 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryMar 22, 2023Corroded; Degraded; Corroded; Degraded

  IT WAS REPORTED THAT THERE WAS APPARENT TRUNNIONOSIS DISCOVERED AFTER REVISION. IT WAS FURTHER REPORTED THAT "PATIENT REPORTED PAIN IN GROIN/ BUTTOCKS AREA. SURGEON REVISED ACETABULUM AND NOTICED WHAT LOOKED TO BE TRUNNIONOSIS ON STEM AND HEAD. DEEP GROVE OF ARTICULATING SURFACE OF LINER WAS NOTICED AND WONDERED WHERE THAT COULD HAVE COME FROM. DISCOLOURATION (YELLOW TINGE) OF LINER IS A CONCERN AS WELL. NO INFECTION WAS PRESENT JUST A LOT OF INFLAMMATION."

  Patient problems: Inflammation; Pain

  MAUDE report 16591006 ↗
• InjuryJun 18, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT PATIENT'S LEFT HIP WAS REVISED. A REP FOR COMPETITOR COVERED THE CASE, THERE WAS NO STRYKER PRESENCE. STRYKER REP REPORTED THAT OUR LFIT C-TAPER FEMORAL HEAD WAS EXPLANTED. A LARGER STRYKER LFIT ANATOMIC C-TAPER FEMORAL HEAD WITH A HIGHER OFFSET AND UNKNOWN COMPETITOR DEVICE(S) WERE IMPLANTED.

  Patient problems: Injury

  MAUDE report 7609472 ↗