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ENDURANCE 1521-73-000Recalls & reported problems

Depuy Orthopaedics, Inc. · FEMORAL STEM 12/14 TAPER ENDURANCE HIP STEM SIZE 3 300mm RIGHT BOWED · Class 2 · Implant

All models of ENDURANCE (20)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295057369), received between Mar 30, 2021 and Mar 30, 2021 — classified as 1 injury.

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

Patient problems

  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryMar 30, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE PATIENT HAD AN ANTIBIOTIC SPACER PLACED ON (B)(6) 2019, PATIENT IS INFECTED AGAIN. STEM AND HEAD WERE REMOVED AGAIN AND ANOTHER ANTIBIOTIC SPACER WAS PLACED. THIS IS ALL THE INFORMATION I HAVE AND CAN GET. DOI: (B)(6) 2019 DOR: (B)(6) 2021 RIGHT HIP.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 11590457 ↗

Other Prosthesis, hip, semi-constrained, metal/polymer, cemented devices

All Prosthesis, hip, semi-constrained, metal/polymer, cemented devices →

Sources and updates

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