REUNION 5573-2E-3602Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07613327098914), received between Sep 5, 2018 and Sep 10, 2026 — classified as 5 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 16, 2026.

Most reported problems

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjurySep 10, 2026Insufficient Device Problem Information

  A Stryker Reunion Reverse shoulder implant was revised using new Stryker Reunion implants.

  Patient problems: Insufficient Information

  MAUDE report 50714930 ↗
• InjuryAug 4, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AS REPORTED: "I AM WRITING TO DRAW YOUR ATTENTION TO A DISTRESSING MEDICAL INCIDENT INVOLVING THE FAILED STRYKER REUNION RIGHT SHOULDER REPLACEMENT SURGERY ON (B)(6) 2020. THE PROCEDURE TOOK PLACE AT (B)(6) MEDICAL CENTER, LOCATED AT (B)(6). REGRETTABLY, DESPITE ENDURING NINE MONTHS OF PERSISTENT PAIN AND LIMITED RANGE OF MOTION, I UNDERWENT REVISION SURGERY ON (B)(6) 2021. PREOPERATIVE DIAGNOSIS: RIGHT SHOULDER FAILED REVERSE TOTAL SHOULDER ARTHROPLASTY, AXILLARY NERVE NEUROPRAXIA. POSTOPERATIVE DIAGNOSIS: CAT SCAN EVALUATION OF THE SHOULDER REVEALED AN OS ACROMIALE AND A FRACTURE LINE AROUND THE HUMERAL ENDOPROSTHESIS WITH PROXIMAL LOOSENING. INITIAL STAGES OF SCAPULAR NOTCHING WAS NOTED. THE METAPHYSEAL PORTION OF THE HUMERAL ENDOPROSTHESIS WAS INFERIOR AND SLIGHTLY MEDIAL TO THE INFERIOR ASPECT OF THE GLENOID. THE CENTER OF ROTATION OF THE REVERSE TOTAL SHOULDER ARTHROPLASTY APPEARED NONLATERALIZED."

  Patient problems: Implant Pain; Loss of Range of Motion; Nerve Damage

  MAUDE report 17460595 ↗
• InjuryFeb 18, 2020Loss of Osseointegration; Loss of Osseointegration

  IT WAS REPORTED THAT THE PATIENT'S LEFT SHOULDER WAS REVISED DUE TO IMPLANT LOOSENING. DUE TO THE PRESENCE OF A HEMATOMA, THE SURGEON REPORTED THAT TRAUMA HAD TO BE A FACTOR. THE PATIENT'S ENTIRE SHOULDER CONSTRUCT EXCEPT FOR THE HUMERAL STEM WAS REVISED. REP REPORTED THAT NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: Hematoma; Injury

  MAUDE report 9722934 ↗
• InjuryMar 29, 2019Device Dislodged or Dislocated

  SURGEON REPORTED THAT LEFT REVERSE SHOULDER REPLACEMENT DUE TO A FRACTURE HAS SUBLUXED AND DISLOCATED. CT SCAN SHOWED LARGE AMOUNT OF FLUID IN THE JOINT. SURGEON DECIDED TO REVISE THE SHOULDER, EVACUATE AND THE FLUID. HE INCREASED THE TENSION WITH INCREASED GLENIOSPHERE OFFSET AND THICKER CUP AND LINER. THE SHOULDER APPEARED STABLE AND THE SURGERY WAS PERFORMED WITHOUT INCIDENT.

  Patient problems: Swelling

  MAUDE report 8466014 ↗
• InjurySep 5, 2018Device Slipped

  IT WAS REPORTED THAT PATIENT'S RIGHT SHOULDER WAS REVISED AFTER PATIENT SUFFERED SEVERAL FALLS AND COMPLAINED OF PAIN. THE GLENOID BASEPLATE WAS FOUND TO HAVE LOOSENED. SURGEON DECIDED TO USE BONE ALLOGRAFT IN THE GLENOID AND A HUMERAL HEAD ON THE EXISTING STEM.

  Patient problems: Fall; Pain

  MAUDE report 7848582 ↗