ENDURANCE 1521-22-000Recalls & reported problems
Depuy Orthopaedics, Inc. · FEMORAL STEM 12/14 TAPER ENDURANCE HIP STEM SIZE 3 190mm LENGTH · Class 2 · Implant
All models of ENDURANCE (20)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 1
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295057260), received between Sep 19, 2017 and Mar 26, 2020 — classified as 1 death, 2 injuries.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).
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
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Insufficient Device Problem Information1
- Loss of or Failure to Bond1
Patient problems
- No Code Available2
- Death1
- Embolism1
- Pain1
- Unspecified Infection1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryMar 26, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
3RD LEFT HIP REVISION. ORIGINAL SURG: (B)(6) 2019; 1ST REV SURG: (B)(6) 2020 (B)(4); 2ND REV SURG; (B)(6) 2020 (B)(4); REMOVED HEAD AND STEM DUE TO INFECTION.
Patient problems: No Code Available; Unspecified Infection
MAUDE report 9884890 ↗InjuryJul 23, 2019Loss of or Failure to Bond; Loss of or Failure to Bond
LITIGATION ALLEGES PAIN AND DIFFICULTY AMBULATING. IN ADDITION TO WHAT WERE PREVIOUSLY ALLEGED, PPF ALLEGES LOOSENING OF THE STEM. ADDED STEM, CEMENTRALIZER AND BONE CEMENT DUE TO LOOSENING. DOI: (B)(6) 2008, DOR: (B)(6) 2010, (LEFT HIP).
Patient problems: No Code Available; Pain
MAUDE report 8816562 ↗DeathSep 19, 2017Insufficient Device Problem Information; Insufficient Device Problem Information
IT WAS REPORTED THAT AFTER IMPLANTING THE REVISION PRODUCTS, THE PATIENT WAS CLOSED UP AND BEGAN EXPERIENCING PROBLEMS. THE PATIENT DIED IN ROOM. THE SURGEON LATER STATED THAT IT WAS PROBABLY DUE TO FAT EMBOLISM. COMPETITOR CEMENT WAS REPORTED TO BE USED DURING THE REVISION.
Patient problems: Death; Embolism
MAUDE report 6876562 ↗
Other Prosthesis, hip, semi-constrained, metal/polymer, cemented devices
- NA 1365-51-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented753 reports
- NA 1365-50-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented412 reports
- ARTICUL/EZE 1365-21-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall280 reports
- ARTICUL/EZE 1365-11-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 death262 reports
- LFIT 6260-9-236Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, cemented256 reports
- PINNACLE GRIPTION 1217-32-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented2 deaths239 reports
- ELEOS™ 25002111EOnkos Surgical, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented3 deaths230 reports
- Novation 130-36-52Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2 recalls124 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.
How reports and recalls are matched · Editorial policy · Report an error on this page