Tornier Perform® Reversed Glenoid DWJ021Recalls & reported problems
Tornier, Inc. · Class 2 · Implant
All models of Tornier Perform Reversed Glenoid (41)
Data updated Oct 16, 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 00846832090365), received between Dec 21, 2022 and Apr 16, 2024 — classified as 2 injuries.
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
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Loss of Range of Motion2
- Bone Fracture(s)1
- Hyperextension1
- Muscle/Tendon Damage1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 16, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A PHS STEMLESS IDE SUBJECT SHOWED MILD ANTERIOR IMPINGEMENT ALONG THE CONJOIN TENDON, EXACERBATED BY HYPEREXTENSION AND MAXIMAL FORWARD FLEXION. TREATMENT INVOLVED A CORTICOSTEROID INJECTION INTO THE CONJOIN TENDON. THE ISSUE'S RELATEDNESS TO THE DEVICE WAS DEEMED POSSIBLE, BUT IT WAS CONSIDERED UNRELATED TO THE SURGERY.
Patient problems: Hyperextension; Loss of Range of Motion; Muscle/Tendon Damage
MAUDE report 19120877 ↗InjuryDec 21, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A PATIENT HAD AN ACROMIAL STRESS FRACTURE. ACTIONS TAKEN CONSISTED OF IMMOBILIZATION AND RESUME PHYSICAL THERAPY. THE PATIENT'S SHOULDER IS VERY STIFF AS A CONSEQUENCE OF THE ACROMIAL STRESS FRACTURE.
Patient problems: Bone Fracture(s); Loss of Range of Motion; Pain
MAUDE report 16022595 ↗
Other PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED devices
- DJO SURGICAL 508-32-204Encore Medical, L.P. · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 recall544 reports
- Comprehensive Reverse Shoulder 010000589Biomet Orthopedics, LLC · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 recall142 reports
- DELTA XTEND 130738203Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED175 reports
- DJO SURGICAL 509-00-432Encore Medical, L.P. · Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented1 recall117 reports
- 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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