FDA Adverse Event Injury Summary report: N

SPRINT QUATTRO SECURE S

MDR report key: 2770963 · Received October 3, 2012

Report

Report Number
2649622-2012-12858
Event Type
Injury
Date Received
October 3, 2012
Date of Event
April 20, 2012
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
LWS
PMA / PMN Number
P920015/S039
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, 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 BY THAT THERE WAS A LEAD WARNING FOR HIGH IMPEDANCE THAT REACHED A MAXIMUM READING OF 2350 OHMS. IT WAS ALSO REPORTED THE LEAD HAD AN APPARENT FRACTURE. THE LEAD WAS REMOVED AND REPLACED. NO PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SPRINT QUATTRO SECURE S IMPLANTABLE TACHY LEAD LWS MEDTRONIC PUERTO RICO, INC. 6935

Patients

Seq Age Sex Outcome Treatment
1 18 YR Hospitalization| R (B)(4) COMPETITOR IMPLANTABLE DEFIBRILLATOR