Continuum® Trabecular Metal™ 00-8757-058-01Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00889024151468), received between Jun 6, 2024 and Feb 18, 2026 — classified as 3 injuries.

The most frequently reported specific device problem is “Malposition of Device” (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 18, 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.

• InjuryFeb 18, 2026Malposition of Device

  IT WAS REPORTED THAT APPROXIMATELY NINE MONTHS POST-IMPLANTATION, THE PATIENT UNDERWENT A RIGHT HIP REVISION DUE TO THE CUP POSITION BEING RETROVERTED. THE PATIENT EXPERIENCED PAIN AND INSTABILITY. PAIN, ANTALGIC GAIN, FORCED EXTERNAL ROTATION IN FLEXION, DIFFICULTY DOING STRAIGHT LEG RAISE, IMPINGEMENT, AND HO WERE ALL OBSERVED DURING PLANNING FOR THE REVISION. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.

  Patient problems: Ambulation or Postural Difficulties; Ankylosis; Extraskeletal ossification; Joint Impingement; Joint Laxity; Pain

  MAUDE report 24379495 ↗
• InjuryJun 25, 2025Material Erosion; Material Erosion

  NO ADDITIONAL EVENT INFORMATION TO REPORT AT THIS TIME.

  Patient problems: Hypersensitivity/Allergic reaction; Metal Related Pathology; Swelling/ Edema

  MAUDE report 22329214 ↗
• InjuryJun 6, 2024Malposition of Device; Noise, Audible; Malposition of Device; Noise, Audible

  IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP PROCEDURE. SUBSEQUENTLY, THE PATIENT WAS REVISED APPROXIMATELY 7 YEARS LATER DUE TO POOR ALIGNMENT OF THE ACETABULAR COMPONENT. THERE WAS REPRODUCIBLE AUDIBLE SQUEAKING AND CREPITUS BY THE PATIENT. IT WAS REPORTED THAT NO FURTHER INFORMATION WAS AVAILABLE.

  Patient problems: Insufficient Information

  MAUDE report 19475386 ↗

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.