FDA Adverse Event Injury Summary report: N

ENRHYTHM DR

MDR report key: 1072536 · Received July 10, 2008

Report

Report Number
2647346-2008-00318
Event Type
Injury
Date Received
July 10, 2008
Date of Event
October 12, 2007
Manufacturer
MEDTRONIC MED REL, INC.
Product Code
DXY
PMA / PMN Number
ASKU
Removal / Correction Number
ASKU
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

ASKU

Description of Event or Problem · 1

ASKU

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ENRHYTHM DR IMPLANTABLE PULSE GENERATOR DXY MEDTRONIC MED REL, INC. P1501DR ASKU

Patients

Seq Age Sex Outcome Treatment
1 79 YR Required Intervention 5072 IMPLANTABLE PACING LEAD