FDA Adverse Event Malfunction Summary report: N

PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

MDR report key: 2951676 · Received February 9, 2013

Report

Report Number
2182208-2013-00079
Event Type
Malfunction
Date Received
February 9, 2013
Date of Event
November 5, 2012
Report Date
November 5, 2012
Manufacturer
RICE CREEK MFG
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

THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. PRODUCT EVENT SUMMARY: THE DEVICE WAS ANALYZED AND NO ANOMALIES WERE FOUND. (B)(4).

Additional Manufacturer Narrative · 1

THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. (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 THE PROGRAMMER IS HAVING A CHALLENGE INTERROGATING PROTECTA XT AND A SENSIA DEVICE. IT DOES NOT APPEAR TO BE PROGRAMMING HEAD RELATED. THE PROGRAMMER AND RADIOFREQUENCY (RF) HEAD WERE RETURNED FOR REPAIR. THE RF HEAD WAS ANALYZED AND TESTED OUT OF SPECIFICATION. THERE WAS NO PATIENT INVOLVEMENT

Description of Event or Problem · 1

IT WAS REPORTED THE PROGRAMMER IS HAVING A CHALLENGE INTERROGATING PROTECTA XT AND A SENSIA DEVICE. IT DOES NOT APPEAR TO BE PROGRAMMING HEAD RELATED. THE PROGRAMMER WAS RETURNED FOR REPAIR. THERE WAS NO PATIENT INVOLVEMENT

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
56242 PULSE-GENERATOR, PACEMAKER, IMPLANTABLE DXY RICE CREEK MFG 2090W

Patients

Seq Age Sex Outcome Treatment
1 2067L RF HEAD 2290 ANALYZER