FDA Adverse Event Injury Summary report: N

OBTAPE TRANSOBTURATOR SLING

MDR report key: 5834195 · Received July 29, 2016

Report

Report Number
1645337-2016-00059
Event Type
Injury
Date Received
July 29, 2016
Report Date
July 20, 2016
Manufacturer
MENTOR WW LLC
Product Code
PAH
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

NOT RETURNED.

Description of Event or Problem · 1

INJURIES. (LITIGATION CASE).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
485967 OBTAPE TRANSOBTURATOR SLING TRANSOBTURATOR PAH MENTOR WW LLC

Patients

Seq Age Sex Outcome Treatment
1 Other