FDA Adverse Event Injury Summary report: N

CAPSUREFIX NOVUS

MDR report key: 1991936 · Received February 15, 2011

Report

Report Number
2649622-2011-02641
Event Type
Injury
Date Received
February 15, 2011
Date of Event
December 10, 2010
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
DTB
PMA / PMN Number
P930039/S009
Removal / Correction Number
ASKU
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
PHYSICIAN

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.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT PRESENTED AT THE EMERGENCY ROOM AFTER RECEIVING SHOCKS PRECEDED BY DIZZINESS, AND MOMENTARILY PASSING OUT. UPON COMING THROUGH, AFTER RECEIVING THE SHOCKS, THE PATIENT WAS NOTED TO BE IN NORMAL SINUS RHYTHM (NSR), WITH LEFT BUNDLE BRANCH BLOCK (LBBB) AND NO BI-VENTRICULAR PACING. IT WAS ALSO NOTED THAT THE PATIENT HAD NO P-WAVES. DEVICE INTERROGATION REVEALED A VENTRICULAR FIBRILLATION EPISODE, AND UPON RECEIVING A SHOCK, ATRIAL SENSING HAD BEEN IMMEDIATELY LOST. IN ADDITION, THE RIGHT VENTRICULAR LEAD EXHIBITED NOISE, AND THE PHYSICIAN WAS SUSPICIOUS OF DEVICE HEADER MALFUNCTION. SEVERAL DAYS LATER, THE RIGHT VENTRICULAR LEAD APPEARED TO HAVE DISLODGED. THE DEVICE, RIGHT VENTRICULAR, AND LEFT VENTRICULAR LEADS WERE EXPLANTED, AND IT WAS NOTED THAT THE IMPLANT POCKET APPEARED TO BE INFECTED. DAYS LATER, A NEW DEVICE AND LEADS WERE IMPLANTED. NO FURTHER PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CAPSUREFIX NOVUS IMPLANTABLE PACING LEAD DTB MEDTRONIC PUERTO RICO, INC. 5076 ASKU

Patients

Seq Age Sex Outcome Treatment
1 56 YR Hospitalization| L| R 1688TC COMPETITOR IMPLANTABLE PACING LEAD