FDA Adverse Event Malfunction Summary report: N

54 CM BIPOLAR LEAD

MDR report key: 3243101 · Received July 18, 2013

Report

Report Number
2183787-2013-00062
Event Type
Malfunction
Date Received
July 18, 2013
Report Date
July 12, 2013
Manufacturer
GREATBATCH MEDICAL
Product Code
DTB
PMA / PMN Number
P130012
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

THE LEAD WAS CAPPED DUE TO NON-CAPTURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
336596 54 CM BIPOLAR LEAD BIPOLAR LEAD DTB GREATBATCH MEDICAL 511212 W2340235

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention