Tornier Perform® Reversed Glenoid DWJ714Recalls & reported problems
Tornier, Inc. · Peripheral 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
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00846832091218), received between Jan 19, 2023 and Sep 11, 2026 — classified as 4 injuries.
The most frequently reported specific device problem is “Loosening of Implant Not Related to Bone-Ingrowth” (2 reports).
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
- Loosening of Implant Not Related to Bone-Ingrowth2
Patient problems
- Insufficient Information2
- Bacterial Infection1
- Unspecified Infection1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjurySep 11, 2026Loosening of Implant Not Related to Bone-Ingrowth
As reported: "Yesterday, the surgeon performed a revision for Pt F G. The glenoid had become unstable and the entire Perform+ construct (baseplate+post+peripheral screws+glenosphere) came out and rotated down. He removed the tray and liner from the humeral components, and due to the stem being well fixed, placed a cobolt-chrome head on instead making it a hemi construct."
Patient problems: Insufficient Information
MAUDE report 50735212 ↗InjurySep 11, 2026Loosening of Implant Not Related to Bone-Ingrowth
As reported: "Yesterday, the surgeon performed a revision for Pt F G. The glenoid had become unstable and the entire Perform+ construct (baseplate+post+peripheral screws+glenosphere) came out and rotated down. He removed the tray and liner from the humeral components, and due to the stem being well fixed, placed a cobolt-chrome head on instead making it a hemi construct."
Patient problems: Insufficient Information
MAUDE report 50735031 ↗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 22154006 ↗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 16203347 ↗
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- 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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