FDA Adverse Event Injury Summary report: N

MEDTRONIC, INC

MDR report key: 507167 · Received January 15, 2004

Report

Report Number
507167
Event Type
Injury
Date Received
January 15, 2004
Date of Event
October 22, 2003
Report Date
December 19, 2003
Manufacturer
MEDTRONIC, INC.
Product Code
LWS
Adverse Event
Yes
Report Source
User Facility report
Reporter Location
MO, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

PACEMAKER DID NOT DISPLAY TELEMETRY AFTER FOUR PROGRAMMER ATTEMPTS TO FIX.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MEDTRONIC, INC ICD LWS MEDTRONIC, INC. 7227CX 270CT03

Patients

Seq Age Sex Outcome Treatment
1 77 YR Required Intervention