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SYNERGY 71306610Recalls & reported problems

Smith & Nephew, Inc. · SYNERGY POROUS COATED FEMORAL SIZE 10 · 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 03596010194442), received between May 18, 2018 and May 18, 2018 — 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

  • Injury1

Recent adverse event reports

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

  • InjuryMay 18, 2018Insufficient Device Problem Information; Insufficient Device Problem Information

    IT WAS REPORTED THAT, THREE MONTHS AFTER IMPLANTING THE CEMENTLESS SYNERGY STEM, X-RAY SHOWED BROKEN STEM.

    Patient problems: Injury

    MAUDE report 7526707 ↗

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

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Sources and updates

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