FDA Adverse Event Injury Summary report: N

2649622-2010-05521

MDR report key: 1992699 · Received February 15, 2011

Report

Report Number
2649622-2010-05521
Event Type
Injury
Date Received
February 15, 2011
Date of Event
March 18, 2010
Report Date
February 25, 2024
Manufacturer
MPRI
PMA / PMN Number
P920015
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Patients

Seq Age Sex Outcome Treatment
1 39 YR Female Hospitalization| R D284VRC ICD