FDA Adverse Event Malfunction Summary report: N

CARELINK PROGRAM W/TELEMETRY C

MDR report key: 2131509 · Received June 16, 2011

Report

Report Number
2182208-2011-00968
Event Type
Malfunction
Date Received
June 16, 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
JA
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 REPORTED EVENT, HOWEVER THE DEVICE POWERED UP WITH A SOFTWARE ERROR.

Description of Event or Problem · 1

THE PROGRAMMER WAS RETURNED TO THE MANUFACTURER DUE TO TELEMETRY FAILURE, ANALYZED AND TESTED OUT OF SPECIFICATION. NO PATIENT INVOLVEMENT OR COMPLICATIONS WERE REPORTED.

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| 2067 PROGRAMMER RF HEAD