Trabecular Metal® 6202-58-20Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889024118959), received between Nov 8, 2022 and Jan 8, 2026 — classified as 4 injuries.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).

3 other recalls cover devices cleared under the same FDA submission (K021891, K093561); they may or may not involve this specific model.

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.

• InjuryJan 8, 2026Loosening of Implant Not Related to Bone-Ingrowth

  IT WAS CONFIRMED THAT NO FURTHER INFORMATION COULD BE PROVIDED.

  Patient problems: Aseptic loosening; Damage to Ligament(s); Joint Dislocation

  MAUDE report 24011627 ↗
• InjuryMar 13, 2025Migration; Migration

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION PROCEDURE 1 YEAR POST IMPLANTATION DUE TO THE CUP SHIFTING POSITIONS. THERE IS NO FURTHER INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Failure of Implant

  MAUDE report 21595238 ↗
• InjuryApr 24, 2024Difficult to Insert; Detachment of Device or Device Component; Difficult to Insert; Detachment of Device or Device Component

  NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.

  Patient problems: Joint Dislocation; Osteolysis

  MAUDE report 19173414 ↗
• InjuryNov 8, 2022Positioning Problem; Positioning Problem

  IT WAS REPORTED A PATIENT UNDERWENT A TOTAL HIP PROCEDURE. DURING THE PROCEDURE, WHILE SECURING THE SHELL, A SCREW SLIPPED ENTIRELY THROUGH THE SCREW HOLE. THERE WAS A DELAY OF FIFTEEN MINUTES WHILE THE SURGEON ATTEMPTED TO REMOVE THE SCREW, BUT WAS UNABLE. THE SCREW REMAINS IN THE PATIENT. DUE DILIGENCE IS IN PROCESS FOR THIS COMPLAINT; TO DATE NO ADDITIONAL INFORMATION HAS BEEN PROVIDED.

  Patient problems: Foreign Body In Patient

  MAUDE report 15754526 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K021891, K093561. One submission often covers many models, so check the product and lot details in each record.

• Z-1496-2014 · Apr 1, 2014 · Terminated
  TRABECULAR METAL MODULAR ACETABULAR SYSTEM, Shell with Cluster Holes, Porous 60mm. Catalog number 00-6202-060-22; Hip implant component.
• Z-3279-2011 · Sep 1, 2011 · Terminated
  The Trabecular Metal Modular Acetabular System is a modular acetabular cup system consisting of a shell with a preassembled locking ring, a liner, and optional screws. The Shells
• Z-0060-2011 · Aug 18, 2010 · Terminated
  Zimmer Trabecular metal Modular Acetabular system 56 mm Porous shell with cluster holes, Catalog 00-6202-056-22, Zimmer Inc., Warsaw, IN. This device is indicated for primary or re