Tornier Perform® Reversed Glenoid DWJ130Recalls & 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 00846832089543), received between Feb 26, 2024 and Sep 27, 2024 — classified as 3 injuries.
The most frequently reported specific device problem is “Loss of Osseointegration” (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
- Loss of Osseointegration1
Patient problems
- Unspecified Infection2
- Inadequate Osseointegration1
- Osteolysis1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjurySep 27, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT UNDERWENT A ONE STAGE REVISION DUE TO AN ACUTE INFECTION.
Patient problems: Unspecified Infection
MAUDE report 20326980 ↗InjuryMar 12, 2024Loss of Osseointegration; Loss of Osseointegration
THE PATIENT INITIALLY HAD A ZB HEMI SHOULDER REPLACEMENT. THE LONG ZB STEM WAS REMOVED, AND A REVIVE WITH PERFORM REVERSE IMPLANT WAS IMPLANTED. THE PATIENT LATER REQUIRED A SECOND REVISION TO A REVIVE HEMI FROM TORNIER REVIVE WITH PERFORM REVERSE DUE TO SIGNIFICANT PROXIMAL BONE RECESSION. THE STEM WAS WELL FIXED, SO EVERYTHING ON THE GLENOID SIDE WAS REMOVED, AND A 52 X 23 FLEX HEAD WAS INSTALLED.
Patient problems: Inadequate Osseointegration; Osteolysis
MAUDE report 18890062 ↗InjuryFeb 26, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE REVISION SURGERY WAS CONDUCTED IN RESPONSE TO AN INFECTION. AN UPDATE PROVIDED INDICATES A LACK OF INFORMATION REGARDING THE LOT NUMBERS FOR THE SCREWS USED. HOWEVER, IT WAS MENTIONED THAT THE INFECTION APPEARED TO BE LOCALIZED, AND THE PROCEDURE INVOLVED WASHING OUT AND EXCHANGING PARTS.
Patient problems: Unspecified Infection
MAUDE report 18778084 ↗
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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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