Trilogy® 00-8753-048-01Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00889024150133), received between Apr 6, 2023 and Sep 9, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Difficult to Insert” (2 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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 9, 2026Inadequacy of Device Shape and/or Size; Positioning Problem

  It was reported that during surgery the size 48 trial cup fit appropriately, but the final implant cup of the same size was excessively loose, requiring upsizing. The surgeon proceeded to implant a size 50 cup.Attempts have been made and no further information has been provided.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50691083 ↗
• MalfunctionApr 6, 2023Difficult to Insert; Difficult to Insert

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16689396 ↗
• MalfunctionApr 6, 2023Difficult to Insert; Difficult to Insert

  IT WAS REPORTED THAT DURING A PROCEDURE, THE LINER WOULD NOT ASSEMBLE WITH THE CUP. ANOTHER LINER AND CUP OF THE SAME SIZE WERE USED, BUT ALSO WOULD NOT ASSEMBLE CORRECTLY. THE SURGEON THEN, REAMED THE BONE A SECOND TIME WITH ONE SIZE GREATER THAN ANTICIPATED AND THESE DEVICES WERE ABLE TO FUNCTION PROPERLY AND WERE IMPLANTED. IT WAS REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE AT THIS TIME.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16689387 ↗

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-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.