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R3 ACETABULAR 71331848Recalls & reported problems

Smith & Nephew, Inc. · R3 0 HOLE ACETABULAR SHELL 48MM · Class 3 · Implant

All models of R3 ACETABULAR (24)

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 03596010597571), received between Dec 21, 2017 and Dec 21, 2017 — 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

  • Joint Dislocation1

Recent adverse event reports

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

  • InjuryDec 21, 2017Insufficient Device Problem Information; Insufficient Device Problem Information

    IT WAS REPORTED THAT A SURGICAL INTERVENTION WAS PERFORMED DUE TO DISLOCATION, ALL PARTS WERE REMOVED.

    Patient problems: Joint Dislocation

    MAUDE report 7140022 ↗

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

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Sources and updates

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