Tornier Perform® Reversed Glenoid DWJ034Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00846832090426), received between Aug 31, 2022 and Sep 17, 2026 — classified as 7 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• InjurySep 17, 2026Unstable

  The manufacturer received a report from the National Joint Registry that contains unpublished collected data on the usage and the outcomes of the shoulder joint replacement.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) 2026.During the review of the report, it was identified that on (b)(6) 2026 a patient required revision surgery due to instability, which was not previously reported to the manufacturer.

  Patient problems: Joint Laxity

  MAUDE report 50803927 ↗
• InjuryMay 15, 2026Device Dislodged or Dislocated

  THE MANUFACTURER RECEIVED A REPORT FROM THE NATIONAL JOINT REGISTRY THAT CONTAINS UNPUBLISHED COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF THE SHOULDER JOINT REPLACEMENT.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) 2026. DURING THE REVIEW OF THE REPORT, IT WAS IDENTIFIED THAT ON (B)(6) 2026 A PATIENT REQUIRED REVISION SURGERY DUE TO DISLOCATION/SUBLUXATION, WHICH WAS NOT PREVIOUSLY REPORTED TO THE MANUFACTURER.

  Patient problems: Subluxation

  MAUDE report 25180907 ↗
• InjuryMar 10, 2026Device Dislodged or Dislocated

  THE MANUFACTURER RECEIVED A REPORT FROM THE NATIONAL JOINT REGISTRY THAT CONTAINS UNPUBLISHED COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF THE SHOULDER JOINT REPLACEMENT.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 BETWEEN 2021 - 2025. DURING THE REVIEW OF THE REPORT, IT WAS IDENTIFIED THAT ON (B)(6) 2025 A PATIENT REQUIRED REVISION SURGERY DUE TO COMPONENT DISSOCIATION AND UNEXPLAINED PAIN, WHICH WAS NOT PREVIOUSLY REPORTED TO THE MANUFACTURER.

  Patient problems: Pain

  MAUDE report 24560491 ↗
• 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 ((B)(4)). 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 23028126 ↗
• InjuryApr 22, 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 OF THE SHOULDER JOINT REPLACEMENT. THE REPORT DETAILS ANALYSIS PROVIDED FOR REVISION PROCEDURES PERFORMED UNTIL (B)(6) 2025. DURING THE REVIEW OF THE REPORT, IT WAS IDENTIFIED THAT ON (B)(6) 2025 A PATIENT REQUIRED REVISION SURGERY DUE TO INFECTION, WHICH WAS NOT PREVIOUSLY REPORTED TO THE MANUFACTURER.

  Patient problems: Unspecified Infection

  MAUDE report 21882345 ↗
• InjuryFeb 6, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THROUGH AN INTERNAL STUDY THAT THE PATIENT ON (B)(6) 2022 EXPERIENCED POST-OPERATIVE COMPLICATION AFTER REVISION SURGERY. THERE WAS PERSISTENT MEDIAL SCAPULAR AND DEEP SHOULDER PAIN. EMG FINDINGS PREOP INDICATED CHRONIC C5 RADICULOPATHY AND DENERVATION OF INFRASPINATUS MUSCLE. THE PATIENT IS TAKING OVER THE COUNTER PAIN MEDICATION.

  Patient problems: Pain

  MAUDE report 16304030 ↗
• InjuryAug 31, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT HAD POSITIVE INTRAOPERATIVE CULTURES THAT WERE MANAGED WITH IV ANTIBIOTICS.

  Patient problems: Unspecified Infection

  MAUDE report 15332041 ↗