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Titan Reverse Shoulder System TRL-0961-05C-SRecalls & reported problems

Smith & Nephew, Inc. · RSS GLENOSPHERE TRIAL. CONCENTRIC-S · Class 1

All models of Titan Reverse Shoulder System (18)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885556864807), received between Sep 7, 2023 and Sep 7, 2023 — classified as 1 malfunction.

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 18, 2026.

Most reported problems

Device problems

  • Fracture1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionSep 7, 2023Fracture; Fracture

    IT WAS REPORTED THAT, DURING A REVERSE SHOULDER ARTHROPLASTY, A RSS GLENOSPHERE TRIAL. CONCENTRIC-S BROKE WHEN IT WAS BEING REMOVED. THE PROCEDURE WAS COMPLETED, WITHOUT ANY DELAY. PATIENT WAS NOT HARMED AS CONSEQUENCE OF THIS PROBLEM.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17698120 ↗

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Sources and updates

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