Tornier Perform® Reversed Glenoid DWJ530Recalls & 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
- 6
- Deaths reported
- 0
- Injuries reported
- 6
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00846832091102), received between Jan 19, 2023 and Jun 24, 2026 — classified as 6 injuries.
The most frequently reported specific device problem is “Break” (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 Problem4
- Break1
- Device Damaged by Another Device1
- Fracture1
- Off-Label Use1
- Osseointegration Problem1
Patient problems
- Unspecified Infection4
- Failure of Implant1
- Fall1
- Inadequate Osseointegration1
- No Clinical Signs, Symptoms or Conditions1
- Post Operative Wound Infection1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
InjuryJun 24, 2026Adverse Event Without Identified Device or Use Problem
REVISION OF ASCEND FLEX REVERSE STEM WITH PERFORM REVERSED GLENOID DUE TO INFECTION
Patient problems: Post Operative Wound Infection
MAUDE report 25604394 ↗InjuryFeb 2, 2026Adverse Event Without Identified Device or Use Problem
SUBJECT: (B)(6). PHS STUDY. REPLACEMENT OF THE COMPLETE PROSTHESIS DUE TO CHRONIC LOW GRADE INFECTION. (LEUKOCYTES 8. G/L, CRP 17.7 MG/L, CELL COUNT: 12,300, 98% POLYNUCLEAR: MIBI FROM PUNCTURE: RENEWED DETECTION OF CUTIBACTERIUM ACNES IN THE CULTURE, PENICILLIN-SENSITIVE).
Patient problems: Unspecified Infection
MAUDE report 24232140 ↗InjuryMay 2, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
AS REPORTED: PHS STUDY SUBJECT: (B)(6). DEEP INFECTION REQUIRING A MEDICAL INTERVENTION (OPENED DEBRIDEMENT AND IRRIGATION). INFECTION C. ACNES. RE-OPERATION WITHOUT IMPLANT EXTRACTION. DATE OF REOPERATION: (B)(6) 2025".
Patient problems: Unspecified Infection
MAUDE report 21948041 ↗InjuryFeb 12, 2024Break; Fracture; Device Damaged by Another Device; Break; Fracture; Device Damaged by Another Device
THE SALES REP REPORTED, "FOLLOWING A PROBLEM WITH THE DMI SHOULDER PROSTHESIS AT THE HOSPITAL, THE BROKEN SCREW AND THE GLENOSPHERE SCREW WERE NOTED INTRAOPERATIVELY." IN ADDITION, THE CUSTOMER REPORTED, "MOBILIZATION OF GLENOSPHERE PLATE + FUNCTIONAL DEGRADATION FOLLOWING A FALL IN (B)(6) 2022- 1 BROKEN SCREW GLENOSPHERE SCREW BROKEN IN CENTRAL SCREW DIFFICULTY IN EXTRACTING BROKEN SCREW FRAGMENT, PREVENTING EXTRACTION OF PLATE FRAGMENT EXTRACTED USING MICROSURGICAL FORCEPS". PATIENT ALSO REQUIRED ANTIBIO-THERAPY DUE TO THE REVISION SURGERY.
Patient problems: Failure of Implant; Fall; No Clinical Signs, Symptoms or Conditions; Unspecified Infection
MAUDE report 18691903 ↗InjuryMay 12, 2023Off-Label Use; Osseointegration Problem; Off-Label Use; Osseointegration Problem
THERE WAS AN EARLY REVISION OF A PERFORM REVERSED GLENOID IMPLANTED. FLUIDS AND TISSUES HAVE BEEN HARVESTED DURING THE REVISION CASE FOR A SUSPECTED INFECTION. THERE IS NO RESULTS OF THE PATHOLOGY TESTS. ONCE THE REVERSE GLENOID WAS REMOVED, THE SURGEON PACKED THE GLENOID VAULT WITH SOME FEMORAL HEAD GRAFT AND HAS CONVERTED THE STEM TO A HEMI PROSTHESIS. THE STEM WAS NOT REVISED.
Patient problems: Inadequate Osseointegration
MAUDE report 16924846 ↗InjuryJan 19, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
INFECTION WAS FOUND IN A PATIENT AFTER ARTIFICIAL SHOULDER JOINT SURGERY.
Patient problems: Unspecified Infection
MAUDE report 16203343 ↗
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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