FDA Adverse Event Injury Summary report: N

OBTAPE

MDR report key: 6135913 · Received November 30, 2016

Report

Report Number
1645337-2016-00204
Event Type
Injury
Date Received
November 30, 2016
Date of Event
November 2, 2016
Report Date
November 29, 2016
Manufacturer
MENTOR WORLDWIDE LLC
Product Code
FTL
Report Source
Manufacturer report
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Description of Event or Problem · 1

INJURIES. LITIGATION CASE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
786058 OBTAPE FTL MENTOR WORLDWIDE LLC 5598134

Patients

Seq Age Sex Outcome Treatment
1