Tornier Perform® Reversed Glenoid DWJ022Recalls & reported problems

Summary

The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00846832090372), received between Nov 4, 2022 and Jun 8, 2026 — classified as 9 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (3 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 9 most recent of 9 reports, in the reporter's own words as published by the FDA.

• InjuryJun 8, 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  THE MANUFACTURER RECEIVED A REPORT FROM THE NATIONAL JOINT REGISTRY THAT CONTAINS UNPUBLISHED COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF THE SHOULDER JOINT REPLACEMENT.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 BETWEEN 2024-2026. DURING THE REVIEW OF THE REPORT, IT WAS IDENTIFIED THAT ON (B)(6) 2026 A PATIENT REQUIRED REVISION SURGERY DUE TO UNEXPLAINED PAIN, WHICH WAS NOT PREVIOUSLY REPORTED TO THE MANUFACTURER.

  Patient problems: Pain

  MAUDE report 25426039 ↗
• InjuryMar 14, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AS REPORTED: "SUBJECT: (B)(6) PERFORM FRACTURE STUDY. POST-OPERATIVE COMPLICATION: MALUNION/NONUNION AT 6M IMAGING APPOINTMENT THE IMAGES SHOW NO BONE CONSOLIDATION."

  Patient problems: Malunion of Bone; Nonunion/Delayed-union Bone Fracture

  MAUDE report 21606334 ↗
• InjuryFeb 26, 2025Unstable; Unstable

  THE MANUFACTURER RECEIVED A REPORT FROM THE NATIONAL JOINT REGISTRY THAT CONTAINS UNPUBLISHED COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF THE SHOULDER REPLACEMENT.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) 2024 A PATIENT REQUIRED REVISION SURGERY DUE TO INSTABILITY WHICH WAS NOT PREVIOUSLY REPORTED TO THE MANUFACTURER. REVISION PROCEDURE TYPE: REVISION STEMMED TOTAL REVERSE ARTHROPLASTY.

  Patient problems: Joint Laxity

  MAUDE report 21468378 ↗
• InjuryFeb 26, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AS REPORTED: "PHS STEMLESS IDE: SUBJECT (B)(6). UNEXPECTED PAIN. SUBJECT'S DOG PULLED SURGICAL ARM ON A WALK CAUSING NUMBNESS, LIMP RIGHT ARM, AND PAIN. BRUISING ON FRONT OF ARM. NUMBNESS AND TINGLING AND WEAKNESS OF ARM IMPROVED WITH REST, BUT REPORTS FEELING TIGHTNESS WITH MOVEMENT. PT REFERRAL PLACED. HAS ONLY ATTENDED ONE PT TREATMENT AS OF REPORT DATE. REPORTS ONGOING PAIN AND STIFFNESS."

  Patient problems: Implant Pain; Loss of Range of Motion; Numbness

  MAUDE report 21468375 ↗
• InjuryMar 4, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THE MANUFACTURER RECEIVED A REPORT FROM THE NATIONAL JOINT REGISTRY THAT CONTAINS UNPUBLISHED COLLECTED DATA ON THE USAGE AND THE OUTCOMES WITH THE TORNIER SHOULDER SYSTEM. THE REPORT DETAILS ANALYSIS PROVIDED FOR PROCEDURES PERFORMED BETWEEN (B)(6)2012 ¿ (B)(6) 2022. DURING THE REVIEW OF THE REPORT, IT WAS IDENTIFIED THAT ON 01-OCTOBER-2021 A PATIENT REQUIRED REVISION SURGERY DUE TO COMPONENT DISSOCIATION , WHICH WAS NOT PREVIOUSLY REPORTED TO THE MANUFACTURER. REVISION PROCEDURE TYPE: SINGLE STAGE REVISION.

  Patient problems: Joint Dislocation

  MAUDE report 18833322 ↗
• InjuryOct 13, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AS REPORTED: "POST-OPERATIVE COMPLICATION: INCREASED PAIN AND DECREASED ROM ACTION(S) TAKEN: MEDICATION: ESTIM, IBUPROFEN, PHYSICAL THERAPY".

  Patient problems: Implant Pain; Loss of Range of Motion

  MAUDE report 17936124 ↗
• InjuryAug 22, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  THE MANUFACTURER RECEIVED A REPORT FROM THE NATIONAL JOINT REGISTRY THAT CONTAINS UNPUBLISHED COLLECTED DATA ON THE USAGE AND THE OUTCOMES WITH THE TORNIER SHOULDER SYSTEM. THE REPORT DETAILS ANALYSIS PROVIDED FOR PROCEDURES PERFORMED BETWEEN APRIL 2012 ¿ MAY 2022. DURING THE REVIEW OF THE REPORT, IT WAS IDENTIFIED THAT ON (B)(6) 2019 A PATIENT REQUIRED REVISION SURGERY DUE TO DISLOCATION AND SUBLUXATION, THE EVENT WAS NOT PREVIOUSLY REPORTED TO THE MANUFACTURER.

  Patient problems: Joint Dislocation

  MAUDE report 17599349 ↗
• InjuryApr 21, 2023Device Dislodged or Dislocated; Adverse Event Without Identified Device or Use Problem; Device Dislodged or Dislocated; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THERE WAS A REVISION SURGERY WITH THE ORIGINAL INTENT ON PERFORMING A SPHERE/POLY SWAP. UPON INSPECTION, PATIENT HAD A LOOSE REVIVE STEM AND NEEDED A NEW ONE. AFTER PREP, THE DECISION WAS MADE TO GO WITH A 130MM FULLY COATED DISTAL STEM INSTEAD OF THE ORIGINAL PARTIALLY COATED STEM. WHEN PUTTING THE 0MM ASSEMBLY SCREW DOWN THE 11MM PROXIMAL BODY, THE 11MM DISTAL STEM WOULDN'T ENGAGE THE SCREW. AFTER MINUTES OF TRYING TO ASSEMBLE WITH NO SUCCESS, THE SCREW WAS NOTICEABLY SHORTER. A 0S SCREW WAS IN THE REGULAR 0MM SKU. THIS CAUSED A TIME DELAY IN CASE. THE PATIENT WAS TOO SMALL TO GO TO A 150MM LENGTH FOR USE. WITH NO OTHER OPTION AVAILABLE, THE PHYSICIAN USED THE 0MM SCREW THAT WAS IN THE ORIGINAL STEM.

  Patient problems: Failure of Implant; Insufficient Information

  MAUDE report 16791993 ↗
• InjuryNov 4, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT HAD POST-OPERATIVE PAIN WHICH LIMITED THEIR RANGE OF MOTION. THROUGH CT SCANS IT WAS REVEALED THAT THE PATIENT HAD INFERIOR OSTEOPHYTE. THE PATIENT UNDERWENT AN ARTHROSCOPIC SURGERY WITHOUT COMPONENT EXTRACTION.

  Patient problems: Extraskeletal ossification; Implant Pain; Loss of Range of Motion

  MAUDE report 15725823 ↗