Tornier Perform® Reversed Augmented Glenoid DWJ504Recalls & reported problems

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00846832092154), received between Aug 31, 2023 and Jun 24, 2026 — classified as 6 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

• InjuryJun 24, 2026Adverse Event Without Identified Device or Use Problem

  REVISION OF ASCEND FLEX REVERSE STEM WITH PERFORM REVERSED GLENOID DUE TO INFECTION

  Patient problems: Post Operative Wound Infection

  MAUDE report 25604389 ↗
• InjurySep 9, 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  THE MANUFACTURER RECEIVED A REPORT FROM THE NATIONAL JOINT REGISTRY THAT CONTAINS UNPUBLISHED COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF THE SHOULDER JOINT REPLACEMENT.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 23001738 ↗
• InjuryJun 5, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE REVERSE SHOULDER ARTHROPLASTY WAS DONE FOR INFECTION. THE SURGEON MENTIONED ENTEROCOCCI WAS DETECTED. THE IMPLANTS WERE REMOVED AND CEMENT SPACER WAS IMPLANTED. NO PRODUCT FAULT WAS REPORTED.

  Patient problems: Bacterial Infection

  MAUDE report 22153903 ↗
• InjuryFeb 26, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AS REPORTED: "PHS STEMLESS IDE: (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 21468386 ↗
• InjurySep 10, 2024Adverse 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 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) 2022 A PATIENT REQUIRED REVISION SURGERY DUE TO INFECTION, WHICH WAS NOT PREVIOUSLY REPORTED TO THE MANUFACTURER. REVISION PROCEDURE TYPE: STAGE 1 OF 2 STAGE REVISION.

  Patient problems: Unspecified Infection

  MAUDE report 20180302 ↗
• InjuryAug 31, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated

  A REVISION SURGERY WAS CONDUCTED USING THE BLUEPRINT PLANNING FEATURE. THE REASON FOR THE REVISION WAS THAT THE PATIENT'S BASEPLATE BECAME DISLODGED FROM THE GLENOID WITHIN TWO WEEKS OF THE INITIAL SURGERY. THE DEVICES REMOVED DURING THE REVISION WERE THE BASEPLATE AND THE GLENOSPHERE. THE INITIAL SURGERY ENCOUNTERED CHALLENGES, INCLUDING A DROP OFF ON THE POSTERIOR GLENOID DUE TO BONE LOSS, WHICH LIKELY CONTRIBUTED TO THE BASEPLATE NOT BEING PROPERLY SECURED. ADDITIONALLY, ONE OF THE PERIPHERAL SCREWS HAD BROKEN DURING THE INITIAL SURGERY, BUT IT WAS NOT DEEMED TO BE THE CAUSE OF THE REVISION.

  Patient problems: Joint Dislocation; Osteopenia/ Osteoporosis

  MAUDE report 17660004 ↗