Tornier Perform® Reversed Glenoid DWJ726Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00846832091249), received between Jul 18, 2022 and Jul 7, 2026 — classified as 7 injuries.

The most frequently reported specific device problem is “Fracture” (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.

Most reported problems

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• InjuryJul 7, 2026Loss of Osseointegration; Adverse Event Without Identified Device or Use Problem

  It was reported that the patient underwent a right primary reverse shoulder arthroplasty. At approximately two-year follow-up, the patient presented with shoulder pain and reduced range of motion. The surgeon noted reported non-compliance with postoperative rehabilitation and a history of potential trauma while climbing in and out of a truck.During revision surgery, the glenoid component was found to be loose and dissociated from the glenoid bone and was easily removed. The humeral component remained well fixed and was retained. The polyethylene insert exhibited eccentric wear, and grey synovial tissue was observed and excised. Copious lavage was performed.New glenoid components were implanted with the addition of synthetic bone graft. A new humeral polyethylene insert was placed. The shoulder was reduced and found to be stable through range of motion.

  Patient problems: Loss of Range of Motion; Pain

  MAUDE report 25734865 ↗
• InjuryMay 29, 2026Fracture; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A RIGHT PRIMARY REVERSE SHOULDER ARTHROPLASTY. AT APPROXIMATELY TWO-YEAR FOLLOW-UP, THE PATIENT PRESENTED WITH SHOULDER PAIN AND REDUCED RANGE OF MOTION. THE SURGEON NOTED REPORTED NON-COMPLIANCE WITH POSTOPERATIVE REHABILITATION AND A HISTORY OF POTENTIAL TRAUMA WHILE CLIMBING IN AND OUT OF A TRUCK. DURING REVISION SURGERY, THE GLENOID COMPONENT WAS FOUND TO BE LOOSE AND DISSOCIATED FROM THE GLENOID BONE AND WAS EASILY REMOVED. THE HUMERAL COMPONENT REMAINED WELL FIXED AND WAS RETAINED. THE POLYETHYLENE INSERT EXHIBITED ECCENTRIC WEAR, AND GREY SYNOVIAL TISSUE WAS OBSERVED AND EXCISED. COPIOUS LAVAGE WAS PERFORMED. NEW GLENOID COMPONENTS WERE IMPLANTED WITH THE ADDITION OF SYNTHETIC BONE GRAFT. A NEW HUMERAL POLYETHYLENE INSERT WAS PLACED. THE SHOULDER WAS REDUCED AND FOUND TO BE STABLE THROUGH RANGE OF MOTION.

  Patient problems: Loss of Range of Motion; Pain

  MAUDE report 25330996 ↗
• InjurySep 18, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT; A PATIENT WAS BOOKING IN FOR A REVISION PROCEDURE DUE TO ONGOING PAIN AND STIFFNESS. DURING THE DISSECTION LOTS OF FLUID/ PUSS WAS SEEN AND THE DECISION WAS MADE TO DO A 2 STAGE PROCEDURE TO CLEAR THE INFECTION. ANOTHER REVISION PROCEDURE WILL BE NEEDED AFTER THE INFECTION HAS CLEARED. NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Loss of Range of Motion; Pain; Unspecified Infection

  MAUDE report 23084247 ↗
• InjuryApr 29, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AS REPORTED: "PATIENT REQUIRED REVISION SURGERY DUE TO INFECTION".

  Patient problems: Unspecified Infection

  MAUDE report 19205365 ↗
• InjuryMar 5, 2024Unstable; Adverse Event Without Identified Device or Use Problem; Unstable; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION SURGERY DUE TO INSTABILITY OF THE JOINT. THE DEVICE WAS REMOVED AND REPLACED WITH NEW HARDWARE.

  Patient problems: Joint Laxity; Unspecified Infection

  MAUDE report 18842504 ↗
• InjuryMay 12, 2023Osseointegration Problem; 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 16924375 ↗
• InjuryJul 18, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT UNDERWENT A REVISION SURGERY DUE TO AN INFECTION 12 MONTHS POST-OP. THE METAL DEVICES WERE REMOVED AND A COMPETITOR'S CEMENT SPACER WAS INSERTED.

  Patient problems: Unspecified Infection

  MAUDE report 15043833 ↗