FDA Adverse Event Malfunction Summary report: N

PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

MDR report key: 2951483 · Received February 9, 2013

Report

Report Number
2182208-2013-00033
Event Type
Malfunction
Date Received
February 9, 2013
Date of Event
November 2, 2012
Report Date
November 2, 2012
Manufacturer
RICE CREEK MFG
Product Code
DXY
PMA / PMN Number
P890003/S080
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

THIS EVENT OCCURRED OUTSIDE THE US WHERE THE SAME MODEL IS DISTRIBUTED. ALL INFORMATION PROVIDED IS INCLUDED IN THIS REPORT. PATIENT INFORMATION IS NOT GENERALLY AVAILABLE DUE TO CONFIDENTIALITY CONCERNS. PRODUCT EVENT SUMMARY: ANALYSIS WAS UNABLE TO CONFIRM THE REPORTED EVENT. INSPECTION OF THE LINK ELECTRONIC MODULE (LEM) AND MAIN PROCESSING UNIT (MPU) CIRCUIT BOARDS REVEALED NO ANOMALIES. THE HARD DRIVE WAS RECONFIGURED AND SOFTWARE WAS RELOADED TO ADDRESS LOGGED SOFTWARE ERRORS. (B)(4).

Additional Manufacturer Narrative · 1

THIS EVENT OCCURRED OUTSIDE THE US WHERE THE SAME MODEL IS DISTRIBUTED. ALL INFORMATION PROVIDED IS INCLUDED IN THIS REPORT. PATIENT INFORMATION IS NOT GENERALLY AVAILABLE DUE TO CONFIDENTIALITY CONCERNS. (B)(4).

Additional Manufacturer Narrative · 1

IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PROGRAMMER POWER SUDDENLY FAILED. THE PROGRAMMER WAS RETURNED FOR SERVICE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PROGRAMMER POWER SUDDENLY FAILED. THE PROGRAMMER WAS RETURNED FOR SERVICE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
57109 PULSE-GENERATOR, PACEMAKER, IMPLANTABLE DXY RICE CREEK MFG 2090

Patients

Seq Age Sex Outcome Treatment
1