Trilogy® 00-8753-052-01Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889024150171), received between May 5, 2022 and Sep 1, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Positioning Failure” (3 reports).

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 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.

• MalfunctionSep 1, 2026Positioning Failure

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50542651 ↗
• MalfunctionMar 14, 2025Difficult to Insert; Difficult to Insert

  NO FURTHER INFORMATION AT THE TIME OF THIS REPORT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21604580 ↗
• MalfunctionMay 10, 2022Positioning Failure; Positioning Failure

  IT WAS REPORTED THAT THE SURGEON PERFORMED THE TESTS WITH THE EVIDENCE MATERIALS AND REQUESTED THE OPENING OF THE IMPLANTS IN QUESTION. AFTER IMPACTION OF THE METALLIC COMPONENT, IT WAS VERIFIED THAT IT PRESENTED LAXITY IN THE ACETABULAR CAVITY. EVEN USING TWO SCREWS TO ESTABLISH THE FIXATION, THE SURGEON DID NOT OBTAIN A SATISFACTORY RESULT AND DECIDED TO REPLACE ALL THE COMPONENTS. NO ADVERSE EVENTS HAVE BEEN REPORTED AS A RESULT OF THE MALFUNCTION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14345943 ↗
• MalfunctionMay 5, 2022Positioning Failure; Positioning Failure

  IT WAS REPORTED THAT AN ACETABULUM 52 WAS OPENED, AND AT THE TIME OF PLACING LINER 36, IT DID NOT FIX INSIDE THE ACETABULUM, SO A NEW LINER 32 WAS OPENED BECAUSE THE MEDICAL TEAM THOUGHT THAT LINER 36 WAS DEFECTIVE. WHEN THEY USED THE LINER 32, IT DIDN'T FIX IT IN THE ACETABULUM EITHER. THE DOCTOR TOOK OUT THE 52 ACETABULUM AND TESTED BOTH LINERS OUTSIDE THE PATIENT, AND NEITHER ONE OF THEM FIXED INSIDE THE ACETABULUM. THEY HAD TO OPEN THE 54 ACETABULUM AND THE 36 LINER TO FINISH THE SURGERY. NO ADVERSE EVENTS HAVE BEEN REPORTED AS A RESULT OF THE MALFUNCTION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14287552 ↗

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.