FDA Adverse Event Injury Summary report: N

OBTAPE TRANSOBTURATOR SLING

MDR report key: 3955192 · Received July 21, 2014

Report

Report Number
1645337-2014-00110
Event Type
Injury
Date Received
July 21, 2014
Report Date
July 2, 2014
Manufacturer
MENTOR WORLWIDE LLC
Product Code
FTL
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
ATTORNEY

Narratives

Description of Event or Problem · 1

INJURIES

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
427503 OBTAPE TRANSOBTURATOR SLING TRANSOBTURATOR FTL MENTOR WORLWIDE LLC

Patients

Seq Age Sex Outcome Treatment
1