FDA Adverse Event Injury Summary report: N

UNK

MDR report key: 2192938 · Received February 20, 2008

Report

Report Number
2192938
Event Type
Injury
Date Received
February 20, 2008
Date of Event
November 8, 2007
Report Date
January 16, 2008
Manufacturer
UNK
Product Code
DXY
Report Source
User Facility report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

(1)PG GENERATOR AND LEADS X2.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 UNK UNK DXY UNK UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 49 YR Hospitalization