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ANTHOLOGY 71356103Recalls & reported problems

Smith & Nephew, Inc. · ANTHOLOGY HIGH OFFSET POROUS SIZE 3 · 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 03596010567857), received between Aug 8, 2017 and Aug 8, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Fracture” (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

  • Fracture1
  • Insufficient Device Problem Information1

Patient problems

  • Bone Fracture(s)1
  • No Code Available1

Recent adverse event reports

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

  • InjuryAug 8, 2017Insufficient Device Problem Information; Fracture; Insufficient Device Problem Information

    IT WAS REPORTED THAT DURING IMPLANTATION OF FEMORAL DEVICE IN TOTAL HIP ARTHROPLASTY A NON-DISPLACED PROXIMAL FEMUR FRACTURE OCCURED. CABLE WAS USED TO RESOLVED THIS ISSUE AND THE SEVERITY WAS DEEMED AS MILD.

    Patient problems: Bone Fracture(s); No Code Available

    MAUDE report 6773581 ↗

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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