EQUINOXE PRIMARY SHOULDER COMPONENTS
Received Jul 21, 2026 · Event occurred Jul 8, 2026
Report 1038671-2026-00923 · MDR key 25887976
Device
Generic name
Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented
Manufacturer
Exactech, Inc.Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
NA · Unknown
- Pain
Narrative
Description of Event or Problem
IT WAS REPORTED THAT A PATIENT WHO HAD A STEMLESS HEMIARTHROPLASTY, UNDERWENT A REVISION PROCEDURE. THE PATIENT WAS COMPLAINING ABOUT PAIN AND HAD A POST-SURGERY INJURY THAT CAUSED DAMAGE TO THE ROTATOR CUFF. THE PATIENT AND SURGEON DISCUSSED AND DECIDED THE BEST CAUSE OF ACTION WAS TO REVISE TO A FULL REVERSE TOTAL SHOULDER. THE HUMERAL STEMLESS CAGE AND HUMERAL HEAD WERE REVISED. THERE WERE NO REPORTED DEVICE BREAKAGES OR SURGICAL DELAYS/PROLONGATIONS. THE PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT.