FDA Adverse Event Malfunction Summary report: N

2183613-2010-00028

MDR report key: 2057707 · Received April 14, 2011

Report

Report Number
2183613-2010-00028
Event Type
Malfunction
Date Received
April 14, 2011
Report Date
November 25, 2024
Manufacturer
MEDTRONIC MILACA, INC.
PMA / PMN Number
P820003
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
BIOMEDICAL ENGINEER
Health Professional
Yes

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown