Trabecular Metal® 00-7864-013-00Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889024139251), received between Mar 30, 2020 and Nov 17, 2025 — classified as 4 injuries.

The most frequently reported specific device problem is “Malposition of Device” (2 reports).

5 other recalls cover devices cleared under the same FDA submission (K051491); 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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryNov 17, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT CALLED IN WITH COMPLAINTS OF LEG DISCREPANCY, PAIN AND RANGE OF MOTION ISSUES FOR THE PAST NINE (9) YEARS. PATIENT HAD A LEFT HIP IMPLANTED NEARLY TEN (10) YEARS AGO AND STATES THE DOCTOR HAS DISMISSED THE CLAIMS MADE. PATIENT WANTS CONFIRMATION THAT THE IMPLANT IS ADEQUATE.

  Patient problems: Loss of Range of Motion; Pain; Unequal Limb Length

  MAUDE report 23569315 ↗
• InjuryApr 18, 2022Malposition of Device; Adverse Event Without Identified Device or Use Problem; Malposition of Device; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THE PATIENT UNDERWENT A LEFT HIP PROCEDURE. SUBSEQUENTLY, THE PATIENT STATES TO HAVE HAD PAIN IN THE GROIN AND BOTH LEGS SINCE THE PROCEDURE. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Pain

  MAUDE report 14137879 ↗
• InjuryApr 18, 2022Malposition of Device; Adverse Event Without Identified Device or Use Problem; Malposition of Device; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THE PATIENT UNDERWENT A RIGHT HIP PROCEDURE. SUBSEQUENTLY, THE PATIENT STATES TO HAVE HAD PAIN IN THE GROIN AND BOTH LEGS SINCE THE PROCEDURE. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

  Patient problems: Pain

  MAUDE report 14137834 ↗
• InjuryMar 30, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  NO ADDITIONAL INFORMATION ON REPORTED EVENT.

  Patient problems: Bone Fracture(s)

  MAUDE report 9897911 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K051491. One submission often covers many models, so check the product and lot details in each record.

• Z-0939-2018 · Jan 3, 2018 · Terminated
  Trabecular Metal Primary Hip Prosthesis; Part Numbers: 1. 00-7864-013-00 (UDI: (01) 00889024139251 (17) 250731 (10) 63703649), and 2. 00-7864-013-20 (UDI: (01) 00889024139268 (17)
• Z-0366-2012 · Nov 16, 2011 · Terminated
  Zimmer ZMR Femoral Spout & Cone Bodies and Trabecular Metal Primary Hip Prosthesis Femoral Stem SIZE 16 171 MM STEM LENGTH 12/14 NECK TAPER - STANDARD BODY - STANDARD NECK OFFSET
• Z-1473-06 · Aug 2, 2006 · Terminated
  Zimmer Trabecular metal primary hip prosthesis femoral stem, press-fit, collarless, 12/14 neck taper - standard body -standard neck offset, size 16, 171 mm stem length, sterile, ti
• Z-1472-06 · Aug 2, 2006 · Terminated
  Zimmer Trabecular metal primary hip prosthesis femoral stem, press-fit, collarless, 12/14 neck taper - standard body -extended neck offset, size 15, 160 mm stem length, sterile, ti
• Z-1471-06 · Aug 2, 2006 · Terminated
  Zimmer Trabecular metal primary hip prosthesis femoral stem, press-fit, collarless, 12/14 neck taper - standard body -extended neck offset, size 14, 149 mm stem length, sterile, ti