FDA Adverse Event Injury Summary report: N

TENSION FREE VAGINAL TAPE

MDR report key: 405809 · Received July 10, 2002

Report

Report Number
2210968-2002-00668
Event Type
Injury
Date Received
July 10, 2002
Date of Event
January 1, 1999
Report Date
June 10, 2002
Manufacturer
MEDSCAND MEDICAL AB
Product Code
FTL
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FI
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED IN THE ACTA OBSTRICA E T GYNECOLOGICA SCANDINAVIA 2002; 81:72-77, THAT THE PT DEVELOPED "DE NOVO" URGE SYMPTOMS AFTER A SLING PROCEDURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TENSION FREE VAGINAL TAPE TVT DEVICE FTL MEDSCAND MEDICAL AB NA UNK

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Required Intervention