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R3 71365152Recalls & reported problems

Smith & Nephew, Inc. · R3 0 DEGREE 32MM INNER DIAMETER TRIAL ACETABULAR LINER 52MM OUTER DIAMETER · Class 1

Data updated Oct 18, 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 03596010599483), received between Jul 17, 2020 and Jul 17, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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 18, 2026.

Most reported problems

Device problems

  • Break1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • InjuryJul 17, 2020Break; Break

    IT WAS REPORTED THAT DURING THR SURGERY THE R3 0DEG 32MM TRIAL 52MM BROKE UPON REMOVAL. THIS HAPPENED OUTSIDE THE PATIENT. NO DELAY. PROCEDURE COULD BE FINISHED USING A S&N BACK UP DEVICE. NO INJURIES REPORTED AT THIS TIME. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 10292414 ↗

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Sources and updates

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