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ANTHOLOGY 71357009Recalls & reported problems

Smith & Nephew, Inc. · ANTHOLOGY STANDARD OFFSET POROUS PLUS HYDROXYAPATITE SIZE 9 · Class 3 · Implant

Data updated Oct 13, 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 03596010559524), received between Sep 16, 2019 and Sep 16, 2019 — classified as 1 injury.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Insufficient Device Problem Information1

Patient problems

  • Unspecified Infection1

Recent adverse event reports

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

  • InjurySep 16, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

    IT WAS REPORTED THAT REVISION SURGERY WAS PERFORMED DUE TO AN INFECTION. THE WHOLE SYSTEM WAS EXPLANTED AND A NEW S&N SYSTEM WAS IMPLANTED.

    Patient problems: Unspecified Infection

    MAUDE report 9070332 ↗

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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