Trilogy® 00-8753-052-02Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889024150188), received between Mar 11, 2022 and Mar 11, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Loosening of Implant Not Related to Bone-Ingrowth” (1 report).

4 other recalls cover devices cleared under the same FDA submission (K091508, K151448, K200823); 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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryMar 11, 2022Loosening of Implant Not Related to Bone-Ingrowth; Migration; Loosening of Implant Not Related to Bone-Ingrowth; Migration

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A HIP REVISION APPROXIMATELY FIVE MONTHS POST IMPLANTATION DUE TO PAIN, LOOSENING OF IMPLANT, AND IMPLANT MIGRATION. OPTIMAL POSITIONING AND AUGMENTATION WITH SCREW CAN BE SEEN ON IMMEDIATE POST OP FILM. FOLLOW UP X-RAYS AT SIX WEEKS POST OP SHOWED CHANGED IN CUP POSITION SECONDARY TO FAILURE OF INGROWTH AND LOOSENING. PATIENT STARTED EXPERIENCING INCREASING HIP PAIN AT FIVE WEEKS POST OP. REVISION WAS FINALLY DONE AFTER A TRIAL OF CONSERVATIVE MANAGEMENT WITH PROTECTED WEIGHT BEARING DID NOT HELP INGROWTH OF CUP. PATIENT CONTINUED TO EXPERIENCE WORSENING PAIN. CUP WAS REVISED. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: Pain

  MAUDE report 13731922 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K091508, K151448, K200823. One submission often covers many models, so check the product and lot details in each record.

• Z-2519-2023 · Jul 26, 2023 · Open, Classified
  M/L Taper Hip Prosthesis Extended Offset, Reduced Neck Length, Size 4 (Item Number 00771100640) and Size 6 (Item Number 00771100440)
• Z-0094-2015 · Oct 1, 2014 · Terminated
  Continuum Acetabular System Trabecular Metal Shell with Multi Holes, Porous 68mm, Prosthesis, Hip, Semi-Constrained, Metal/Polymer
• Z-0071-2011 · Mar 19, 2010 · Terminated
  Continuum Acetabular Systems Shell Inserter Adapter with Rotational Control, 00-8790-003-00, Zimmer Inc., Warsaw, IN. Used to mate the inserter with the shell implant.
• Z-0072-2011 · Mar 19, 2010 · Terminated
  Continuum Acetabular Systems Shell Inserter Adapter without Rotational Control, 00-8790-003-10, Zimmer Inc., Warsaw, IN. Used to mate the inserter with the shell implant.