Trabecular Metal® 00-7864-014-20Recalls & reported problems
Zimmer, Inc. · Class 2 · Implant
All models of Trabecular Metal (74)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00889024139282), received between Apr 15, 2024 and Aug 25, 2025 — classified as 4 injuries.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem4
Patient problems
- Bursitis4
- Pain2
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryAug 25, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL HIP PROCEDURE. SUBSEQUENTLY, THE PATIENT REPORTED TENDERNESS OVER THE GREATER TROCHANTER CONSISTENT WITH BURSITIS APPROXIMATELY 1 YEAR LATER. THE PATIENT WAS USING CANES TO AMBULATE AND EXPERIENCED A MODERATE LIMP. THE SURGEON PROVIDED A CORTISONE INJECTION AND A TOPICAL ANTI-INFLAMMATORY CREAM, AND THE ISSUES WERE REPORTEDLY RESOLVED. ATTEMPTS HAVE BEEN MADE, AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Bursitis; Pain
MAUDE report 22884462 ↗InjuryDec 4, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE INITIAL RIGHT TOTAL HIP ARTHROPLASTY. APPROXIMATELY 2 YEARS LATER THE PATIENT RECEIVED A CORTISONE INJECTION TO THE RIGHT HIP FOR BURSITIS AND PAIN. SYMPTOMS WERE REPORTED AS RESOLVED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Bursitis; Pain
MAUDE report 20846757 ↗InjurySep 12, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED 2 YEARS AND 2 MONTHS POST IMPLANTATION, THE PATIENT WAS GIVEN A CORTISONE INJECTION FOR LEFT HIP BURSITIS. THE BURSITIS WAS LIKELY RELATED TO THE INITIAL PROCEDURE. THERE ARE NO PLANS FOR THE PATIENT TO BE REVISED. ALL DEVICES REMAIN IMPLANTED. THERE IS NO ADDITIONAL INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
Patient problems: Bursitis
MAUDE report 20205032 ↗InjuryApr 15, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT APPROXIMATELY 2 YEARS POST IMPLANTATION OF A LEFT TOTAL HIP ARTHROPLASTY, THE PATIENT RECEIVED A CORTISONE INJECTION FOR MILD PAIN IN THE TROCH BURSA, WHICH RELIEVED THE PAIN. THE SURGEON REPORTED THAT TROCHANTERIC BURSITIS IS EXTREMELY COMMON AFTER HIP REPLACEMENT AND IS NOT CONSIDERED A COMPLICATION. THERE WERE NO PRECEDENT FACTORS FOR THIS PATIENT OTHER THAN NORMAL EVERYDAY USE OF THE HIP. NO ADDITIONAL INFORMATION AVAILABLE.
Patient problems: Bursitis
MAUDE report 19105114 ↗
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 · TerminatedTrabecular 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 · TerminatedZimmer 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 · TerminatedZimmer 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 · TerminatedZimmer 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 · TerminatedZimmer 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
Other PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED devices
- PINNACLE 1217-25-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED735 reports
- NA 1365-52-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED683 reports
- APEX 1246-03-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED3 deaths613 reports
- PINNACLE 1217-20-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED2 deaths590 reports
- PINNACLE 1217-30-500Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 death484 reports
- NA 1365-53-000Depuy (Ireland) · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED404 reports
- PINNACLE ALTRX 1221-36-054Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED388 reports
- PINNACLE ALTRX 1221-32-050Depuy Orthopaedics, Inc. · PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED386 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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