FDA Adverse Event Injury Summary report: N

ADVANTAGE SYSTEM

MDR report key: 2961771 · Received February 14, 2013

Report

Report Number
3005099803-2013-00939
Event Type
Injury
Date Received
February 14, 2013
Report Date
January 29, 2013
Manufacturer
BOSTON SCIENTIFIC - MARLBOROUGH
Product Code
FTL
PMA / PMN Number
K020110
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT THE PATIENT WAS IMPLANTED WITH AN ADVANTAGE TRANSVAGINAL MID-URETHRAL SLING SYSTEM DURING A PROCEDURE ON (B)(6) 2008. ACCORDING TO THE COMPLAINANT, POST-PROCEDURE, THE PATIENT EXPERIENCED COMPLICATIONS (SPECIFICS UNKNOWN). ACCORDING TO THE PHYSICIAN, NO COMPLICATIONS WERE ENCOUNTERED DURING THE PROCEDURE AND THERE WERE NO POST-PROCEDURAL COMPLAINTS FROM THE PATIENT. HE LAST SAW THE PATIENT IN (B)(6) 2012. ALL OTHER INFORMATION IS UNKNOWN. SHOULD ADDITIONAL RELEVANT DETAILS BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
64572 ADVANTAGE SYSTEM MESH, SURGICAL, POLYMERIC FTL BOSTON SCIENTIFIC - MARLBOROUGH UNK557

Patients

Seq Age Sex Outcome Treatment
1 Other