FDA Adverse Event Injury Summary report: N

AEQUALIS KEELED GLENOID UNKNOWN

MDR report key: 4687505 · Received April 8, 2015

Report

Report Number
9610667-2015-00030
Event Type
Injury
Date Received
April 8, 2015
Report Date
March 19, 2015
Manufacturer
TORNIER SAS
Product Code
HSD
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THIS IS THE FINAL REPORT SUBMITTED REGARDING THIS SURGICAL EVENT AND MEDICAL DEVICE. "WALCH G, MORAGA C, ET AL. (2012). RESULTS OF ANATOMIC NONCONSTRAINED PROSTHESIS IN PRIMARY OSTEOARTHRITIS WITH BICONCAVE GLENOID", J SHOULDER ELBOW SURG, 21:1526-1533.

Description of Event or Problem · 1

DUE TO POSTERIOR PROSTHESIS DISLOCATION, 1 PATIENT UNDERWENT A REOPERATION TO REORIENTATE THE GLENOID AND PERFORM A POSTERIOR CAPSULORRHAPHY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
230603 AEQUALIS KEELED GLENOID UNKNOWN NONE HSD TORNIER SAS

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention