FDA Adverse Event Injury Summary report: N

OBTAPE TRANSOBTURATOR SLING

MDR report key: 3901453 · Received June 19, 2014

Report

Report Number
1645337-2014-00102
Event Type
Injury
Date Received
June 19, 2014
Report Date
June 19, 2014
Manufacturer
MENTOR WORLDWIDE LLC
Product Code
OTN
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

MULTIPLE INJURIES INCLUDING BUT NOT LIMITED TO URINARY INCONTINENCE, VAGINAL IRRITATION, PAINFUL INTERCOURSE AND EROSION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
361825 OBTAPE TRANSOBTURATOR SLING TRANSOBTURATOR OTN MENTOR WORLDWIDE LLC

Patients

Seq Age Sex Outcome Treatment
1 Other