TRABECULAR METAL™ 00-7000-062-20Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889024310902), received between Oct 7, 2021 and Mar 10, 2025 — classified as 4 injuries.

The most frequently reported specific device problem is “Off-Label Use” (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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryMar 10, 2025Off-Label Use; Off-Label Use

  NO FURTHER INFORMATION IS AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Joint Dislocation

  MAUDE report 21559449 ↗
• InjuryJul 10, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THERE IS NO UPDATE TO THE PRIOR EVENT DESCRIPTION PROVIDED.

  Patient problems: Failure of Implant; Osteolysis

  MAUDE report 17289204 ↗
• InjuryOct 26, 2021Unstable; Unstable

  IT WAS REPORTED THE PATIENT UNDERWENT LEFT THA DUE TO FEMORAL NECK FRACTURE. SUBSEQUENTLY, PATIENT WAS REVISED TWO DAYS LATER DUE TO AN IATROGENIC ACETABULAR FRACTURE. THE PATIENT UNDERWENT A SECOND REVISION APPROXIMATELY 4 MONTHS LATER DUE TO PAIN AND INSTABILITY WITH PLACEMENT OF A CUSTOM CAGE AND CONSTRAINED LINER. DURING THE REVISION, SIGNIFICANT SCARRING WAS NOTED WHICH PROMPTED THE REMOVAL OF THE FEMORAL COMPONENT. THE ACETABULAR COMPONENT WAS FOUND WELL FIXED AND INGROWN. THE CEMENTED LINER WAS REMOVED AS WELL AS THE CUP. BACKING OUT THE SCREWS WAS NOT POSSIBLE, SO THE SURGEON CUT THEM WITH A BUR SO THAT THE CUSTOM CAGE COULD BE PLACED. DUE TO INTRAOPERATIVE COMPLICATIONS, ONLY THE CUSTOM CAGE, LINER, AND SCREWS WERE PLACED. THE WOUND WAS CLOSED WITHOUT FEMORAL COMPONENTS IN PLACE, AND THE PATIENT WAS TRANSFERRED TO THE CRITICAL CARE UNIT. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Pain; Scar Tissue; Swelling/ Edema

  MAUDE report 12697114 ↗
• InjuryOct 7, 2021Osseointegration Problem; Osseointegration Problem

  NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Failure of Implant

  MAUDE report 12589947 ↗