Trabecular Metal® 6202-52-22Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00889024118881), received between Mar 19, 2021 and Aug 11, 2023 — classified as 3 injuries.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryAug 11, 2023Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information; Adverse Event Without Identified Device or Use Problem; Insufficient Device Problem Information

  IT WAS REPORTED THAT THE PATIENT HAD AN INITIAL HIP ARTHROPLASTY. SUBSEQUENTLY, THE PATIENT HAD AN ADDITIONAL PROCEDURE DUE TO TWO TORN TENDONS OF THE RIGHT HIP SIX (6) MONTHS POST IMPLANTATION. NO IMPLANTS WERE REMOVED. NO COMPLAINT OF ANYTHING WRONG WITH THE IMPLANTS.

  Patient problems: Insufficient Information; Muscle/Tendon Damage

  MAUDE report 17508538 ↗
• InjuryJun 15, 2022Malposition of Device; Malposition of Device

  IT WAS REPORTED THAT PATIENT UNDERWENT A LEFT HIP REVISION AFTER APPROXIMATELY 4 YEARS POST IMPLANTATION DUE TO LINER WEAR. THE CUP, LINER AND HEAD WERE REMOVED AND REPLACED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Failure of Implant

  MAUDE report 14692831 ↗
• InjuryMar 19, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  UPON REASSESSMENT OF THE REPORTED EVENT, IT WAS DETERMINED TO BE NOT REPORTABLE. THE INITIAL REPORT WAS FORWARDED IN ERROR AND SHOULD BE VOIDED.

  Patient problems: Insufficient Information

  MAUDE report 11528873 ↗

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