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ANTHOLOGY 71357101Recalls & reported problems

Smith & Nephew, Inc. · ANTHOLOGY HIGH OFFSET POROUS PLUS HYDROXYAPATITE SIZE 1 · Class 3 · Implant

All models of ANTHOLOGY (69)

Data updated Oct 16, 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 03596010559562), received between Jun 16, 2021 and Jun 16, 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 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Metal Related Pathology1
  • Unspecified Infection1

Recent adverse event reports

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

  • InjuryJun 16, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT, AFTER A BHR THA WAS PERFORMED ON (B)(6) 2008, THE PATIENT EXPERIENCED INFECTION AND METALLOSIS. A REVISION SURGERY WAS PERFORMED ON (B)(6) 2021 TO TREAT THESE ADVERSE EVENTS. ALL THE COMPONENTS WERE EXPLANTED. IT IS UNKNOWN IF THE PATIENT RECEIVED ANY MEDICATION TO TREAT THE INFECTION. THE PATIENT OUTCOME IS UNKNOWN.

    Patient problems: Metal Related Pathology; Unspecified Infection

    MAUDE report 12011075 ↗

Other Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented devices

All Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented devices →

Sources and updates

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