FDA Adverse Event Summary report: N

EP IMPLANT TRAY

MDR report key: 4093809 · Received September 11, 2014

Report

Report Number
4093809
Date Received
September 11, 2014
Date of Event
August 27, 2014
Report Date
September 11, 2014
Manufacturer
MEDICAL ACTION INDUSTRIES, INC.
Product Code
FSM
Report Source
User Facility report
Reporter Location
FL, US

Narratives

Description of Event or Problem · 1

THE IMPLANT TRAY WAS MISSING THE SUCTION TUBING AND CAUTERY PEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
563251 EP IMPLANT TRAY TRAY, SURGICAL FSM MEDICAL ACTION INDUSTRIES, INC. * *

Patients

Seq Age Sex Outcome Treatment
1 *