FDA Adverse Event Other Summary report: N

BARD COMPOSIX KUGEL MESH PATCH - EXPANSION

MDR report key: 1661623 · Received April 16, 2010

Report

Report Number
MW5015570
Event Type
Other
Date Received
April 16, 2010
Report Date
April 12, 2010
Product Code
FTM
Report Source
Voluntary report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

I'M SENDING THIS MEDICAL REPORT BECAUSE I'VE HAD THIS PATCH SINCE 2003 AND STILL TODAY I'M HAVING SEVERE REOCCURRING SYMPTOMS. I HAD REOCCURRING SURGERY. I'VE HAD ALL SYMPTOMS LISTED. I THOUGHT I WAS LOSING MY MIND. TILL MY DAUGHTER WHO WORKS FOR FDA FINALLY, INVESTIGATED. RIGHT NOW THIS MESH IS KILLING ME. I NEED SURGERY RIGHT AWAY. PLEASE HELP BEFORE I DIE. I CAN NO LONGER ABSORB OR EAT FOOD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BARD COMPOSIX KUGEL MESH PATCH - EXPANSION NONE FTM

Patients

Seq Age Sex Outcome Treatment
1