Trilogy® 00-8753-050-01Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889024150157), received between Sep 4, 2019 and Nov 3, 2023 — classified as 1 injury, 3 malfunctions.

The most frequently reported specific device problem is “Difficult to Insert” (2 reports).

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 16, 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.

• MalfunctionNov 3, 2023Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT THE LINER WOULD NOT SEAT IN THE CUP. THEY ATTEMPTED TO SEAT IT FOR 3 HOURS WHEN THEY FINALLY CONCLUDED THAT THE PROCEDURE NEEDED TO BE COMPLETED USING NEW DEVICES. THERE IS NO ADDITIONAL INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18064656 ↗
• MalfunctionJul 25, 2022Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THE LINER COULD NOT BE ASSEMBLED WITH THE CUP. A DUAL MOBILITY WAS USED INSTEAD. A 30 MINUTE DELAY OCCURRED. NO ADVERSE EVENTS HAVE BEEN REPORTED AS A RESULT OF THIS MALFUNCTION. ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15100120 ↗
• MalfunctionMar 4, 2021Positioning Failure; Positioning Failure

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11411859 ↗
• InjurySep 4, 2019Device Contaminated During Manufacture or Shipping; Packaging Problem; Device Contaminated During Manufacture or Shipping; Packaging Problem

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

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8961116 ↗

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-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.