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Tornier Perform® Reversed Augmented Glenoid DWJ513Recalls & reported problems

Tornier, Inc. · Class 2 · Implant

All models of Tornier Perform Reversed Augmented Glenoid (8)

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 00846832092086), received between Jul 12, 2023 and Jul 12, 2023 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Bone Fracture(s)1
  • Pain1

Recent adverse event reports

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

  • InjuryJul 12, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT A PATIENT HAD A SCAPULAR FRACTURE. PATIENT EXPERIENCED SHOULDER PAIN. PATIENT CONTACTED SURGEON AND WAS INSTRUCTED TO GO TO ER FOR X-RAYS. NO FRACTURE READILY EVIDENT. PATIENT RETURNED TO CLINIC FOR SOC AND STUDY VISIT. RADIOGRAPHS CLEARLY SHOWED ACROMIAL STRESS FRACTURE WITHOUT ANGULATION NOR DISPLACEMENT OF THE FRACTURE. THE ACROMIAL STRESS FRACTURE IS HEALING WELL.

    Patient problems: Bone Fracture(s); Pain

    MAUDE report 17304728 ↗

Other PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED devices

All PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED devices →

Sources and updates

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