Skip to content

ANTHOLOGY 71357010Recalls & reported problems

Smith & Nephew, Inc. · ANTHOLOGY STANDARD OFFSET POROUS PLUS HYDROXYAPATITE SIZE 10 · 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 03596010559531), received between Feb 20, 2020 and Feb 20, 2020 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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.

  • InjuryFeb 20, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

    IT WAS REPORTED THAT A REVISION WAS PERFORMED DUE TO DEEP INFECTION, PAIN, AVAL AND PSEUDOTUMOR.

    Patient problems: Unspecified Infection

    MAUDE report 9733880 ↗

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

How reports and recalls are matched · Editorial policy · Report an error on this page