Please click on and read the following 2 links from the FDA regarding why we have to register our surgery experience
on a Worldwide Registry. The
greater the number who register the greater the chance of getting this Mesh and these Devices off the Market. Thank you.
Dated 20th October 2008
FDA - Information on Surgical Mesh for Pelvic Organ Prolapse and Stress Urinary Incontinence
http://www.fda.gov/MedicalDevices/Safety/AlertsandNotices/ucm142636.htm
FDA - Public Health Notification: Serious Complications Associated with Transvaginal Placement of Surgical Mesh in Repair of Pelvic Organ Prolapse and Stress Urinary Incontinence
http://www.fda.gov/MedicalDevices/Safety/AlertsandNotices/PublicHealthNotifications/ucm061976.htm
To date October 2008 the FDA USA has received 1000 adverse reports on their Manufacturer and User Facility Device Experience Database MAUDE database. Here is the link to submit your surgery details
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/search.CFM
FDA MedWatch https://www.accessdata.fda.gov/scripts/medwatch/medwatch-online.htm
Your privacy is taken seriously here at Truth in Medicine all submissions are treated as strictly confidential and will not be shared with third parties without your written consent and permission.
