Trilogy® 00-8753-046-01Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024150119), received between Jun 1, 2020 and Sep 4, 2025 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Device-Device Incompatibility” (1 report).

3 other recalls cover devices cleared under the same FDA submission (K091508, K151448); 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 4, 2025Positioning Failure; Device-Device Incompatibility; Positioning Failure; Device-Device Incompatibility

  IT WAS REPORTED THAT DURING THE PROCEDURE; THE 28 MM LINER COULD NOT BE IMPLANTED INTO THE SIZE FF/46 CUP. AFTER SEVERAL ATTEMPTS, THE LINER WOULD NOT IMPLANT AND THE CUP WAS LOOSENING. THE FIRST CUP WAS REMOVED AND A LARGER CUP IMPLANTED. A 32 MM LINER WAS ATTEMPTED TO BE USED AND WOULD NOT IMPLANT. A CERAMIC LINER WAS ABLE TO BE USED TO COMPLETE THE PROCEDURE. THERE WAS A 30-MINUTE DELAY. THERE WAS NO KNOWN IMPACT OR CONSEQUENCES TO THE PATIENT. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22963931 ↗
• InjuryJun 1, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  UPON RECEIPT OF ADDITIONAL INFORMATION IT HAS BEEN DETERMINED THAT THE REPORTED DEVICE DID NOT CAUSE OR CONTRIBUTE TO THE EVENT.

  Patient problems: Unspecified Infection

  MAUDE report 10106742 ↗

Recalls under the same FDA submission

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

• 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-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.
• 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.