Continuum® Trabecular Metal™ 00-8757-058-02Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889024151475), received between May 13, 2021 and Dec 8, 2021 — classified as 2 injuries.

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

• InjuryDec 8, 2021Migration; Migration

  IT WAS REPORTED THAT PATIENT UNDERWENT INITIAL HIP ARTHROPLASTY. SUBSEQUENTLY, PATIENT WAS REVISED 2 YEARS POST IMPLANTATION FOR ASEPTIC LOOSENING. CONTINUUM CUP EXPLANTED AND REPLACED WITH A CUP FROM ANOTHER COMPANY. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Failure of Implant

  MAUDE report 12960855 ↗
• InjuryMay 13, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT PRESENTED TO PHYSICIAN APPROXIMATELY 2 WEEKS POST INITIAL RIGHT HIP PROCEDURE WITH LATERAL REDNESS IN A WELL-APPROXIMATED, ALMOST HEALED INCISION. THE PATIENT WAS PLACED ON ORAL ANTIBIOTICS AND INSTRUCTED TO RETURN IN ONE WEEK FOR A FOLLOW UP. UPON RETURN, IT WAS NOTED THAT THE INCISION WAS COMPLETELY HEALED. NO FURTHER COMPLICATIONS WERE REPORTED CONCERNING THE INCISION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Impaired Healing

  MAUDE report 11819984 ↗

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.