Tornier Perform® Reversed Glenoid DWJ540Recalls & reported problems
Tornier, Inc. · Central Screw · Class 2 · Implant
All models of Tornier Perform Reversed Glenoid (41)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00846832091126), received between Sep 5, 2024 and Feb 6, 2026 — classified as 5 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem3
- Device Dislodged or Dislocated1
- Unstable1
Patient problems
- Bacterial Infection1
- Joint Laxity1
- Medical device site infection1
- Subluxation1
- Unspecified Infection1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryFeb 6, 2026Device Dislodged or Dislocated
IT WAS REPORTED THAT, THE PRIMARY SURGERY WAS CONDUCTED ON (B)(6) 2025. DISLOCATION OF THE GLENOID COMPONENT WAS REPORTED. THE IMPACT ON PAIN AND RANGE OF MOTION WAS UNCLEAR. THE PHYSICIAN COMMENTED THAT THE CAUSE WAS THE PATIENT'S BONE QUALITY ISSUES AND THE INHERENTLY LOW BONE STOCK IN THE GLENOID CAVITY. IMAGES OF X-RAY ARE UNAVAILABLE. THE REVISION SURGERY WAS CONDUCTED ON (B)(6) 2026.
Patient problems: Subluxation
MAUDE report 24280098 ↗InjurySep 11, 2025Unstable; Unstable
IT WAS REPORTED THAT, THE CONVERSION OF REVERSE TOTAL SHOULDER ARTHROPLASTY TO HEMIARTHROPLASTY WAS PERFORMED. SECOND REVISION OF PERFORM HUMERAL STEM AND PERFORM REVERSE GLENOID FOR CHRONIC DISLOCATION (INSTABILITY). INDEX SURGERY DONE IN USA. THE PATIENT DISLOCATED AGAIN 4 WEEKS AFTER THE REVISION DONE ON (B)(6) 2025 (OA 1156009). THE PERFORM REVERSE 42 + 4MM ECCENTRIC GLENOSPHERE, 4 X PERIPHERAL SCREWS, +3MM LATERALISED BASEPLATE AND 40MM X 6.5MM CENTRAL SCREW WERE EXPLANTED. THE 10 DEGREE 42MM RETENTIVE +6MM LINER WAS EXPLANTED AND THE HUMERAL PROSTHESIS WAS CONVERTED TO A HEMI-ARTHROPLASTY WITH A CENTRED HUMERAL HEAD COUPLER AND 43 X 16MM PERFORM HUMERAL HEAD.
Patient problems: Joint Laxity
MAUDE report 23028206 ↗InjuryJun 5, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE REVERSE SHOULDER ARTHROPLASTY WAS DONE FOR INFECTION. THE SURGEON MENTIONED ENTEROCOCCI WAS DETECTED. THE IMPLANTS WERE REMOVED AND CEMENT SPACER WAS IMPLANTED. NO PRODUCT FAULT WAS REPORTED.
Patient problems: Bacterial Infection
MAUDE report 22153904 ↗InjuryApr 8, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
REVISION FOR SUSPECTED INFECTION. REMOVAL OF ALL IMPLANTS (REVERSE SHOULDER REPLACEMENT) AND IMPLANTATION OF CEMENT SPACER.
Patient problems: Medical device site infection
MAUDE report 21796945 ↗InjurySep 5, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE MANUFACTURER RECEIVED A REPORT FROM THE NATIONAL JOINT REGISTRY THAT CONTAINS UNPUBLISHED COLLECTED DATA ON THE USAGE AND THE OUTCOMES WITH THE TORNIER SHOULDER SYSTEM. THE REPORT DETAILS ANALYSIS PROVIDED FOR PROCEDURES PERFORMED BETWEEN APRIL 2012 ¿ MAY 2022. DURING THE REVIEW OF THE REPORT, IT WAS IDENTIFIED THAT ON (B)(6) 2021 A PATIENT REQUIRED REVISION SURGERY DUE TO INFECTION, WHICH WAS NOT PREVIOUSLY REPORTED TO THE MANUFACTURER. REVISION PROCEDURE TYPE: DEBRIDEMENT AND IMPLANT RETENTION (DAIR).
Patient problems: Unspecified Infection
MAUDE report 20144657 ↗
Other shoulder prosthesis, reverse configuration devices
- DJO SURGICAL 508-36-101Encore Medical, L.P. · shoulder prosthesis, reverse configuration508 reports
- DJO SURGICAL 508-32-101Encore Medical, L.P. · shoulder prosthesis, reverse configuration433 reports
- DJO SURGICAL 508-32-103Encore Medical, L.P. · shoulder prosthesis, reverse configuration421 reports
- DJO SURGICAL 509-00-036Encore Medical, L.P. · shoulder prosthesis, reverse configuration1 recall259 reports
- DJO SURGICAL 508-32-104Encore Medical, L.P. · shoulder prosthesis, reverse configuration1 recall203 reports
- DJO SURGICAL 509-00-032Encore Medical, L.P. · shoulder prosthesis, reverse configuration233 reports
- DELTA XTEND 130760000Depuy (Ireland) · shoulder prosthesis, reverse configuration223 reports
- DJO SURGICAL 508-00-032Encore Medical, L.P. · shoulder prosthesis, reverse configuration122 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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