FDA Adverse Event Injury Summary report: N

4261806

MDR report key: 4261806 · Received November 12, 2014

Report

Report Number
4261806
Event Type
Injury
Date Received
November 12, 2014
Date of Event
October 14, 2014
Report Date
November 7, 2014
Adverse Event
Yes
Product Problem
Yes
Report Source
User Facility report
Reporter Location
VA, US

Patients

Seq Age Sex Outcome Treatment
0 72 YR Hospitalization| R