FDA Adverse Event Malfunction Summary report: N

CARELINK PROGRAM W/TELEMETRY C

MDR report key: 2813170 · Received October 31, 2012

Report

Report Number
2182208-2012-03873
Event Type
Malfunction
Date Received
October 31, 2012
Manufacturer
MEDTRONIC, INC.
Product Code
DXY
PMA / PMN Number
P890003/S080
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THIS REPORT IS BASED SOLELY ON DEVICE RETURN AND ANALYSIS. NO INFORMATION TO SUGGEST A DEVICE-RELATED ADVERSE EVENT OR PRODUCT PROBLEM WAS RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. EVALUATION SUMMARY: (B)(4): ANALYSIS FOUND THAT THE PROGRAMMER FAN WAS NOISY, THE ELECTROCARDIOGRAM (ECG) CONNECTOR WAS LOOSE AND THE MICROPHONE WAS OUT OF ELECTRICAL SPECIFICATION.

Description of Event or Problem · 1

IT WAS REPORTED THE PROGRAMMER FAN IS VERY NOISY. THE PROGRAMMER WAS RETURNED FOR REPAIR. IT WAS ANALYZED AND TESTED OUT OF SPECIFICATION. THERE WAS NO PATIENT INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CARELINK PROGRAM W/TELEMETRY C PROGRAMMER DXY MEDTRONIC, INC. 2090W

Patients

Seq Age Sex Outcome Treatment
1 Other 2067 PROGRAMMER RF HEAD