FDA Adverse Event Malfunction Summary report: N

3871413

MDR report key: 3871413 · Received May 14, 2014

Report

Report Number
3871413
Event Type
Malfunction
Date Received
May 14, 2014
Date of Event
April 29, 2014
Report Date
May 13, 2014
Product Problem
Yes
Report Source
User Facility report
Reporter Location
MA, US
Reporter Occupation
RISK MANAGER

Patients

Seq Age Sex Outcome Treatment
1 81 YR