FDA Adverse Event Malfunction Summary report: N

2183613-2010-00026

MDR report key: 1876792 · Received October 20, 2010

Report

Report Number
2183613-2010-00026
Event Type
Malfunction
Date Received
October 20, 2010
Report Date
November 25, 2024
Manufacturer
MEDTRONIC MILACA, INC.
PMA / PMN Number
P820003
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MS, US
Reporter Occupation
OTHER

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown