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Tornier Perform® Anatomic Glenoid DWE422Recalls & reported problems

Tornier · CortiLoc® Pegged Glenoid · Class 2 · Implant

All models of Tornier Perform Anatomic Glenoid (25)

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 03700434021844), received between Jul 16, 2024 and Jul 16, 2024 — classified as 1 injury.

The most frequently reported specific device problem is “Osseointegration Problem” (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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 1 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Osseointegration Problem1

Patient problems

  • Inadequate Osseointegration1
  • Osteolysis1

Recent adverse event reports

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

  • InjuryJul 16, 2024Osseointegration Problem; Osseointegration Problem

    AS REPORTED: "GLENOID COMPONENT LOOSENING. ASEPTIC GLENOID FAILURE. INVESTIGATOR REVIEW OF IMAGES ON 21 DEC 2023 VISIT: NOTE NO COMPONENT MIGRATION, BUT NOTED HUMERAL OSTEOLYSIS AT ZONE 6, 7, AND 8 >2CM AND GLENOID OSTEOLYSIS AT ZONES 3, 5 AND 6 >2MM. REVISION SURGERY ON (B)(6) 2024".

    Patient problems: Inadequate Osseointegration; Osteolysis

    MAUDE report 19756687 ↗

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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