Tornier Perform® Anatomic Glenoid DWE433Recalls & reported problems
Tornier · CortiLoc® Pegged Glenoid · Class 2 · Implant
All models of Tornier Perform Anatomic Glenoid (25)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 03700434022575), received between Jan 31, 2022 and Mar 7, 2022 — classified as 2 injuries.
The most frequently reported specific device problem is “Loosening of Implant Not Related to Bone-Ingrowth” (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
- Loosening of Implant Not Related to Bone-Ingrowth1
- Loss of Osseointegration1
Patient problems
- Implant Pain2
- Loss of Range of Motion1
- Osteolysis1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMar 7, 2022Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth
IT WAS REPORTED THAT THE PATIENT HAS BEEN COMPLAINING OF PAIN AND LOSS OF MOTION. XRAYS SHOWED EXTENSIVE LUCENCY AROUND THE GLENOID COMPONENT AND LOOSENING WAS CONFIRMED DURING THE SURGERY. THE STEM, HUMERAL HEAD AND GLENOID COMPONENT WERE REMOVED AND REVISED.
Patient problems: Implant Pain; Loss of Range of Motion; Osteolysis
MAUDE report 13685323 ↗InjuryJan 31, 2022Loss of Osseointegration; Loss of Osseointegration
IT WAS REPORTED THAT PATIENT (B)(6) UNDERWENT A REVISION SURGERY 10 YEARS AFTER PRIMARY STUDY SURGERY DUE TO GLENOID COMPONENT LOOSENING. (PATIENT NOTICED WORSENING PAIN SINCE (B)(6) 2021 AND CT SCAN SHOWS SEVERE LUCENCY AND BONE LOSS SURROUNDING THE GLENOID COMPONENT AND A NON DISPLACED ACROMION FRACTURE). THE GLENOID COMPONENT WAS REMOVED AND BONE GRAFTED.
Patient problems: Implant Pain
MAUDE report 13392046 ↗
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- Alliance® SBGL3007Zimmer, Inc. · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED162 reports
- DELTA XTEND 130760138Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED146 reports
- DELTA XTEND 130790030Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED132 reports
- DJO SURGICAL 509-00-436Encore Medical, L.P. · Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented124 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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