MAUDE Adverse Event Report: MPRI SUREFIX; ELECTRODE, PACEMAKER, PERMANENT

Model Number	5072-45
Medical Device Problem Codes	Failure to Capture (1081); Under-Sensing (1661); High Capture Threshold (3266)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Product analysis the full lead was returned in segments, analyzed, and no anomalies were found.Visual summary analysis of the lead indicated apparent explant damage.
Event or Problem Description
It was reported that the patient's right ventricular (rv) lead had oversensing, noise with high rate non sustained episodes.The lead was explanted and replaced.As well, the patient's right atrial (ra) lead experienced high thresholds, non capture, and complete undersensing.The lead was explanted and replaced.No patient complications have been reported as a result of this event.
Additional Manufacturer Narrative
If information is provided in the future, a supplemental report will be issued.

• Brand Name: SUREFIX
• Common Device Name: ELECTRODE, PACEMAKER, PERMANENT
• Manufacturer (Section D): MPRI; road 149 km 56.3; villalba PR 00766
• MDR Report Key: 6470660
• Report Number: 2649622-2017-04034
• Device Sequence Number: 16226378
• Product Code: DTB
• UDI-Device Identifier: 00885074311869
• UDI-Public: 00885074311869
• Combination Product (Y/N): N
• Initial Reporter State: OK
• Initial Reporter Country: US
• PMA/510(K) Number: P930039
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2012
• Device Explanted Year: 2017
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 01/18/2017

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Lay User/Patient
• Device Expiration Date: 11/02/2012
• Device Model Number: 5072-45
• Device Catalogue Number: 5072-45
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 01/23/2017
• Initial Date Received by Manufacturer: 01/18/2017
• Supplement Date Received by Manufacturer: 01/18/2017
• Initial Report FDA Received Date: 04/06/2017
• Supplement Report FDA Received Date: 09/29/2017
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: 6947M62 LEAD, DTBB1D4 ICD
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention
• Patient Age: 56 YR