Tornier Perform® Reversed Augmented Glenoid DWJ512Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00846832092079), received between Apr 26, 2022 and Jan 28, 2026 — classified as 6 injuries.

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

Most reported problems

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjuryJan 28, 2026Adverse 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  THE MANUFACTURER RECEIVED A REPORT FROM THE NATIONAL JOINT REGISTRY THAT CONTAINS UNPUBLISHED COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF THE SHOULDER JOINT REPLACEMENT. THE REPORT DETAILS ANALYSIS PROVIDED FOR REVISION PROCEDURES PERFORMED UNTIL (B)(6) 2024. DURING THE REVIEW OF THE REPORT, IT WAS IDENTIFIED THAT ON (B)(6) 2023, A PATIENT REQUIRED REVISION SURGERY DUE TO INFECTION, WHICH WAS NOT PREVIOUSLY REPORTED TO THE MANUFACTURER.

  Patient problems: Unspecified Infection

  MAUDE report 24197660 ↗
• InjurySep 11, 2025Unstable; Unstable

  IT WAS REPORTED THAT, THE CONVERSION OF REVERSE TOTAL SHOULDER ARTHROPLASTY TO HEMIARTHROPLASTY WAS PERFORMED. SECOND REVISION OF PERFORM HUMERAL STEM AND PERFORM REVERSE GLENOID FOR CHRONIC DISLOCATION (INSTABILITY). INDEX SURGERY DONE IN USA. THE PATIENT DISLOCATED AGAIN 4 WEEKS AFTER THE REVISION DONE ON (B)(6) 2025 (OA 1156009). THE PERFORM REVERSE 42 + 4MM ECCENTRIC GLENOSPHERE, 4 X PERIPHERAL SCREWS, +3MM LATERALISED BASEPLATE AND 40MM X 6.5MM CENTRAL SCREW WERE EXPLANTED. THE 10 DEGREE 42MM RETENTIVE +6MM LINER WAS EXPLANTED AND THE HUMERAL PROSTHESIS WAS CONVERTED TO A HEMI-ARTHROPLASTY WITH A CENTRED HUMERAL HEAD COUPLER AND 43 X 16MM PERFORM HUMERAL HEAD.

  Patient problems: Joint Laxity

  MAUDE report 23028251 ↗
• InjuryNov 19, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE SURGEON USED THE BASEPLATE INSERTER TO ATTEMPT TO REMOVE A BASEPLATE. THE BASEPLATE WAS WELL FIXED AND IT DEFORMED THE BASEPLATE INSERTER. REMOVAL WAS DUE TO PATIENT INFECTION.

  Patient problems: Unspecified Infection

  MAUDE report 20727467 ↗
• 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 8/7/24 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 20298704 ↗
• InjuryJan 30, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IN THE PHS STEMLESS IDE STUDY, A PARTICIPANT REPORTED STIFFNESS AND DISCOMFORT IN THE NECK AND LEFT HAND. DESPITE RECEIVING TREATMENTS LIKE MELOXICAM AND ORAL STEROIDS, THE SYMPTOMS PERSISTED. SEEKING A SECOND OPINION FROM A HAND SPECIALIST, THE PATIENT UNDERWENT A STEROID INJECTION IN THE LEFT RING AND LONG FINGERS. DISSATISFIED WITH THE PROGRESS AND CARE, THE PARTICIPANT WAS REFERRED TO ANOTHER HAND SURGEON FOR FURTHER EVALUATION, INCLUDING PENDING EMG AND CERVICAL MRI. THE PATIENT ATTRIBUTES THE SYMPTOMS TO A PREVIOUS SHOULDER SURGERY, EXPRESSING CERTAINTY THAT IT IS THE ROOT CAUSE.

  Patient problems: Discomfort; Loss of Range of Motion

  MAUDE report 18609102 ↗
• 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 14206480 ↗