Tornier Perform® Reversed Glenoid DWJ125Recalls & 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
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00846832090242), received between Jul 16, 2024 and Jun 19, 2025 — classified as 3 injuries.
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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
- Osseointegration Problem1
Patient problems
- Bone Fracture(s)2
- Pain2
- Implant Pain1
- Inadequate Osseointegration1
- Loss of Range of Motion1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryJun 19, 2025Osseointegration Problem; Osseointegration Problem
IT WAS REPORTED THAT THE PATIENT'S STATUS IS POST RIGHT REVERSE TOTAL SHOULDER ARTHROPLASTY. ONE OF THE SCREWS FROM THE IMPLANTS CAME LOOSE AND FRACTURED THE SCAPULA, CAUSING PAIN.
Patient problems: Bone Fracture(s); Inadequate Osseointegration; Pain
MAUDE report 22294313 ↗InjuryDec 12, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
AS REPORTED: "SUBJECT: (B)(6). SCAPULAR FRACTURE. PT WAS DOING PLATES AND STRENGTH TRAINING WITH SUDDEN ONSET OF SEVERE LEFT SHOULDER PAIN GOING FROM SORE TO UNABLE TO RAISE LEFT ARM. PATIENT WAS DIAGNOSED WITH AN ACROMIAL FRACTURE (B)(6) 2024 AND RETURNED TO CLINIC (B)(6) 2024 WITH SHOULDER RECOVERING. ACTIONS TAKEN: REHABILITATION (BONE STIMULATOR) & TREATMENT/MEDICATION (SLING AT ALL TIMES, 3-4 WEEKS, DICLOFENAC AND TYLENOL FOR MILD TO MODERATE PAIN). AE UPDATE (B)(6) 2024 DESCRIPTION OF UPDATE: PATIENT HAS RECOVERED WELL AND CLINIC TEAM HAS ADVISED SHE CONTINUES TO TRANSITION INTO ALL ACTIVITIES AS TOLERATED WHILE USING BONE STIMULATOR FOR ANOTHER 6 WEEKS."
Patient problems: Bone Fracture(s); Implant Pain; Loss of Range of Motion
MAUDE report 20913247 ↗InjuryJul 16, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
AS REPORTED: "ADVERSE EVENT DESCRIPTION: UNEXPECTED PAIN NOT RELATED TO SURGICAL RECOVERY. PATIENT CONTACTED CLINICAL TEAM AFTER HAVING SORENESS AND SOME MOVEMENT LIMITATION IN STUDY SHOULDER. ON 05/13, PATIENT REPORTED THE SYMPTOMS HAD SUBSIDED."
Patient problems: Pain
MAUDE report 19755938 ↗
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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