Tornier Perform® Reversed Glenoid DWJ024Recalls & reported problems

Summary

The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00846832090396), received between Apr 26, 2022 and May 23, 2025 — classified as 9 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (4 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 16, 2026.

Most reported problems

Recent adverse event reports

The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.

• InjuryMay 23, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE MANUFACTURER RECEIVED A REPORT FROM THE NATIONAL JOINT REGISTRY THAT CONTAINS UNPUBLISHED COLLECTED DATA ON THE USAGE AND THE OUTCOMES WITH THE SHOULDER JOINT REPLACEMENT. THE REPORT DETAILS ANALYSIS PROVIDED FOR PROCEDURES PERFORMED UNTIL (B)(6) 2024. DURING THE REVIEW OF THE REPORT, IT WAS IDENTIFIED THAT ON (B)(6) 2020, A PATIENT REQUIRED REVISION SURGERY DUE TO INFECTION WHICH WAS NOT PREVIOUSLY REPORTED TO THE MANUFACTURER.

  Patient problems: Unspecified Infection

  MAUDE report 22078587 ↗
• InjuryNov 28, 2024Osseointegration Problem; Osseointegration Problem

  AS REPORTED: "SUBJECT (B)(6) SHOUT - TORNIER SHOULDER OUTCOMES STUDY. COMPONENT LOOSENING. SUBJECT HAD A CT SCAN PERFORMED AND IT WAS NOTED THAT THE GLENOID COMPONENT WAS LOOSE."

  Patient problems: Inadequate Osseointegration

  MAUDE report 20804617 ↗
• InjuryNov 28, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AS REPORTED: "SUBJECT (B)(6) SHOUT - TORNIER SHOULDER OUTCOMES STUDY. SHOULDER PAIN SUBJECT IS EXPERIENCING DISCOMFORT IN THE SHOULDER. PER CALL WITH SITE ON 31-OCT-2024, VERBALLY REVIEWED ADDITIONAL CLINIC NOTES: ¿ AUG 2023, NO CHANGE RADIOGRAPHICALLY (ONGOING), ¿ MARCH 2024 WORSENING PAIN, NO LOOSENING AND NO CHANGE IN ALLOGRAFT, LUCENCY AROUND BASEPLATE, BUT NO SHIFTING OF POSITION (ONGOING)".

  Patient problems: Discomfort; Implant Pain

  MAUDE report 20804608 ↗
• InjuryNov 14, 2024Unstable; Device Dislodged or Dislocated; Unstable; Device Dislodged or Dislocated

  AS REPORTED: "PHS STUDY SUBJECT: (B)(6). COMPLICATION DESCRIPTION: INSTABILITY/DISLOCATION PATIENT HAS HAD CONTINUED INSTABILITY OF RIGHT RSA DESPITE FORMALIZED PT. PATIENT REVISED ON (B)(6) 2024."

  Patient problems: Joint Laxity; Subluxation

  MAUDE report 20681015 ↗
• InjuryOct 11, 2024Unstable; Device Dislodged or Dislocated; Unstable; Device Dislodged or Dislocated

  AS REPORTED: "STUDY: SHOUT SUBJECT: (B)(6). POST-OPERATIVE AE: INSTABILITY ¿ DISLOCATION SUBJECT WAS AT WORK AND CAUGHT A LARGE 100 LB CRATE. RIGHT SHOULDER DISLOCATED DURING THIS EVENT. REVISION SURGERY WITH REMOVAL OF 4 PROSTHETIC COMPONENTS ON (B)(6) 2024."

  Patient problems: Joint Laxity; Subluxation

  MAUDE report 20426068 ↗
• InjurySep 25, 2024Unstable; Device Dislodged or Dislocated; Unstable; Device Dislodged or Dislocated

  AS REPORTED: "STUDY: SHOUT SUBJECT: (B)(6). POST-OPERATIVE AE: INSTABILITY ¿ DISLOCATION. SUBJECT LIFTED LARGE WATER BOTTLE ON (B)(6) 2024 AND FELT A POP. IMAGING SHOWED DISLOCATED RSA. PATIENT REQUIRED REVISION SURGERY. RE-OPERATION WITH COMPONENT CHANGE ON (B)(6) 2024".

  Patient problems: Joint Laxity; Subluxation

  MAUDE report 20298696 ↗
• 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 NEW HARDWARE.

  Patient problems: Joint Laxity; Unspecified Infection

  MAUDE report 18842449 ↗
• InjuryApr 21, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT UNDERWENT LEFT REVERSE SHOULDER REPLACEMENT ON (B)(6) 2023. PATIENT'S SHOULDER DISLOCATED TWO DAYS LATER, WHICH WAS MANIPULATED AND A CLOSED REDUCTION ACHIEVED. PATIENT AGAIN DISLOCATED THEIR PROSTHETIC SHOULDER TWO DAYS LATER. DECISION MADE TO OPEN WOUND UP, AND DETERMINE CAUSE OF INSTABILITY. ALSO, PATIENT'S WOUND RETURNED A POSITIVE SWAB FOR "COLONIZATION" ACCORDING TO SURGEON. DURING SURGERY, MULTIPLE TISSUE SPECIMENS WERE TAKEN, FOR PATHOLOGY. AN OSTEOPHYTE OF THE POSTERO-SUPERIOR ASPECT OF THE PROXIMAL HUMERUS WAS IDENTIFIED AS THE LIKELY CAUSE OF THE RANGE OF MOTION IMPINGEMENT, LEADING TO INSTABILITY / DISLOCATION. THIS WAS REMOVED; THE GLENOSPHERE WAS EXCHANGED (AS THERE WERE MINOR SCRATCHES ON THE POLISHED SURFACE). THE 6MM POLY WAS ALSO EXCHANGED FOR A 9MM POLY, WHICH CONFERRED GREATER STABILITY, AND ADEQUATELY TENSIONED THE JOINT. STABLE RANGE OF MOTION OBTAINED; WOUND CLOSED. BOTH EXPLANTED PROSTHESIS DISCARDED BY SCRUB NURSE.

  Patient problems: Joint Dislocation; Unspecified Infection

  MAUDE report 16792079 ↗
• InjuryApr 26, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT FELL ON ICE AND GOT A DISLOCATED SHOULDER. THE EMERGENCY ROOM WAS UNABLE TO RELOCATE SHOULDER SO THE PATIENT STAYED OVERNIGHT AND THEN WAS TAKEN TO THE OPERATING ROOM NEXT MORNING FOR RELOCATION UNDER ANESTHESIA. THE PATIENT REMAINS PSEUDOPARALYTIC AND WILL BE WORKED UP FOR A REVISION RSA.

  Patient problems: Fall; Joint Dislocation; Loss of Range of Motion

  MAUDE report 14206472 ↗