Tornier Perform® Reversed Glenoid DWJ346Recalls & 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
- 3
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00846832089819), received between Jan 25, 2023 and Jun 19, 2025 — classified as 2 injuries, 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break2
- Fracture2
- Mechanical Jam1
- Osseointegration Problem1
Patient problems
- Bone Fracture(s)1
- Foreign Body In Patient1
- Inadequate Osseointegration1
- No Clinical Signs, Symptoms or Conditions1
- Pain1
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 IS STATUS 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 22294358 ↗InjuryAug 31, 2023Break; Fracture; Break; Fracture
IT WAS REPORTED A PERIPHERAL SCREW HAD BROKEN DURING AN INITIAL SURGERY. THE BROKEN SCREW WAS LEFT IN THE PATIENT.
Patient problems: Foreign Body In Patient
MAUDE report 17660006 ↗MalfunctionJan 25, 2023Break; Fracture; Mechanical Jam; Break; Fracture; Mechanical Jam
IT WAS REPORTED THAT 3 PERIPHERAL SCREWS BROKE OFF AT THE NECK OF THE SCREW WHILE IMPLANTING. ALL 3 INCIDENT HAVE BEEN THE EXACT SAME SCENARIO IN ALL 3 CASES THE SURGEON DRILLED THE PERIPHERAL SCREW HOLE AND THEN MEASURED FOR SCREW DEPTH AND STARTED TO IMPLANT CORRESPONDING SCREW. ONCE THE SCREW WAS ABOUT 90% IMPLANTED IT WOULD STOPPED TURNING. THE SURGEON IN EACH SCENARIO THEN ATTEMPTED TO BACK OUT THE SCREW AND IT WOULD NOT BACK OUT OR ADVANCE ANY MORE. THE SURGEON THEN CONTINUED TRYING TO BACK OUT THE SCREW UNTIL IT FINALLY SNAPPED 3-4 THREADS DOWN THE SCREW. THE SURGEON WENT ABOUT A NORMAL TECHNIQUE TO COMPLETE THE SURGERY. ALL THE DEBRIS WAS SUCCESSFULLY REMOVED FROM THE FIELD/PATIENT. PRODUCTS WILL NOT BE RETURNING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16240509 ↗
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.
How reports and recalls are matched · Editorial policy · Report an error on this page