FDA Adverse Event Malfunction Summary report: N

CARELINK PROGRAM W/TELEMETRY C

MDR report key: 2207907 · Received August 11, 2011

Report

Report Number
2182208-2011-01721
Event Type
Malfunction
Date Received
August 11, 2011
Manufacturer
MEDTRONIC, INC.
Product Code
DXY
PMA / PMN Number
P890003/S080
Removal / Correction Number
ASKU
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THIS EVENT OCCURRED OUTSIDE THE US. ALL INFORMATION PROVIDED IS INCLUDED IN THIS REPORT. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. PATIENT INFORMATION IS NOT GENERALLY AVAILABLE DUE TO CONFIDENTIALITY CONCERNS. EVALUATION SUMMARY (B)(4): ANALYSIS COULD NOT CONFIRM THE ALLEGATION; HOWEVER, THE RIGHT ANTENNA TESTED OUT OF SPECIFICATION. IT WAS ALSO NOTED THAT THE SYSTEM FAN WAS NOISY AND THE POWER SUPPLY FAN.

Description of Event or Problem · 1

IT WAS REPORTED A VITATRON DEVICE COULD NOT BE INTERROGATED, EVEN THOUGH THE PROGRAMMER WAS SWITCHED TO THE VITATRON SCREEN. NO PATIENT INVOLVEMENT OR COMPLICATIONS WERE REPORTED AS A RESULT OF THIS EVENT.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 Other 2290 PACING SYSTEM ANALYZER