GLENOID BASEPLATE
Received Jul 21, 2026 · Event occurred Apr 28, 2026
Report 0008031020-2026-00895 · MDR key 25895604
Device
Generic name
Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented
Manufacturer
Stryker GmbhCatalog number
5572-2802
Lot number
UNKNOWN
Product problems
- Osseointegration Problem
Patient
83 YR · Female
- Joint Impingement
Narrative
Description of Event or Problem
IT WAS REPORTED THAT, SEVEN YEARS POSTOPERATIVELY, THE IMPLANT DEVELOPED IMPINGEMENT. DURING THE REVISION PROCEDURE, THE EXISTING BASEPLATE WAS REMOVED AND REPLACED WITH AN ARTHREX BASEPLATE POSITIONED AT THE MOST INFERIOR ASPECT OF THE GLENOID. PREOPERATIVE RADIOGRAPHS INDICATED THAT THE 6.5 MM CENTRAL SCREW APPEARED FRACTURED. FOLLOWING REMOVAL OF THE BASEPLATE, INTRAOPERATIVE C-ARM IMAGING CONFIRMED THAT A PORTION OF THE SCREW REMAINED IN THE GLENOID. A SMALL BURR WAS USED TO WIDEN THE OPENING, AND A TREPHINE WAS THEN USED TO REMOVE THE RETAINED SCREW FRAGMENT.
Additional Manufacturer Narrative
SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE, IT WILL BE PROVIDED IN A SUPPLEMENTAL REPORT.