FDA Adverse Event Injury Summary report: N

SPRINT QUATTRO

MDR report key: 3153660 · Received June 8, 2013

Report

Report Number
2649622-2013-06152
Event Type
Injury
Date Received
June 8, 2013
Report Date
March 28, 2013
Manufacturer
MPRI
Product Code
LWS
PMA / PMN Number
P920015
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
RI, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

PRODUCT EVENT SUMMARY: THE PARTIAL LEAD IN SEGMENTS WAS RETURNED AND ANALYZED. A PROXIMAL PORTION WAS RECEIVED MEASURING 49.5 CM. A DISTAL PORTION WAS RECEIVED MEASURING 49.5 CM. ANALYSIS WAS PERFORMED AND NO ANOMALIES WERE FOUND. VISUAL SUMMARY ANALYSIS OF THE LEAD INDICATED APPARENT EXPLANT DAMAGE.

Additional Manufacturer Narrative · 1

THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. 7278 IMPLANTABLE PACEMAKER/CARDIO/DEFIB - 2005 (B)(6); 4592-53 IMPLANTABLE PACING LEAD - 2003 (B)(6). (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT WAS BEING HOSPITALIZED FOR SEPTICEMIA AND THEIR DEVICE HAS NOT BEEN CHECKED SINCE (B)(6) 2010. UPON INTERROGATION OF THE PATIENT'S DEVICE IT WAS FOUND THAT THE RIGHT VENTRICULAR LEAD HAD HIGH IMPEDANCE, INCREASED THRESHOLD, AND OVERSENSING. THE LEAD WAS EXPLANTED. IT WAS ALSO REPORTED THAT DUE TO THE PATIENT'S SEPSIS THE DEVICE AND THE ATRIAL LEAD WERE ALSO REMOVED. IT WAS ALSO NOTED THAT THE DEVICE WAS APPROACHING ELECTIVE REPLACEMENT INDICATOR (ERI). NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
256452 SPRINT QUATTRO DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER LWS MPRI 694465

Patients

Seq Age Sex Outcome Treatment
1 00061 YR Hospitalization| R