FDA Adverse Event Malfunction Summary report: N

9610175-2014-00072

MDR report key: 3574382 · Received January 14, 2014

Report

Report Number
9610175-2014-00072
Event Type
Malfunction
Date Received
January 14, 2014
Date of Event
December 1, 2013
Report Date
January 4, 2014
Manufacturer
FRANTZ MEDICAL DEVELOPMENT LTD.
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
NOT APPLICABLE
Health Professional
N

Patients

Seq Age Sex Outcome Treatment
1 Unknown