inforMED
InjuryKWS

EQUINOXE PRIMARY SHOULDER COMPONENTS

Received Jul 15, 2026

Report 1038671-2026-00894 · MDR key 25829780

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 · Female

  • Arthropathy

Narrative

Description of Event or Problem

IT WAS REPORTED THAT A PATIENT WHO HAD AN INITIAL RIGHT TOTAL SHOULDER ARTHROPLASTY UNDERWENT A REVISION PROCEDURE APPROXIMATELY 8 MONTHS POST. THE PATIENT HAD A SUCCESSFUL TOTAL SHOULDER ARTHROPLASTY BUT HAS SINCE HAD CUFF FAILURE CAUSING THE SURGEON TO REVISE TO A REVERSE. PROVIDED IMAGES SHOW WEAR OF THE GLENOID COMPONENT. THE IMPLANTS WERE REMOVED AND REPLACED WITHOUT COMPLICATION. THERE WAS NO REPORTED BREAKAGE OF A DEVICE OR SURGICAL DELAY/PROLONGATION. THE PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT.