FDA Adverse Event Malfunction Summary report: N

7951123

MDR report key: 7951123 · Received October 10, 2018

Report

Report Number
7951123
Event Type
Malfunction
Date Received
October 10, 2018
Date of Event
October 2, 2018
Report Date
October 3, 2018
Product Problem
Yes
Report Source
User Facility report
Reporter Location
AZ
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

THE SURGEON HAD DIFFICULTY DEPLOYING THE FALOPE RING.

Patients

Seq Age Sex Outcome Treatment
1 10585 DA