FDA Adverse Event Injury Summary report: N

SPRINT QUATTRO SECURE

MDR report key: 1810112 · Received August 20, 2010

Report

Report Number
2649622-2010-05472
Event Type
Injury
Date Received
August 20, 2010
Date of Event
March 18, 2010
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
LWS
PMA / PMN Number
P920015/S24
Removal / Correction Number
ASKU
Report Source
Manufacturer report
Reporter Location
DE, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

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 THE LEAD IMPEDANCE VARIED FROM 400 TO 1200 OHMS. IT WAS ALSO REPORTED THAT DURING INTERROGATION, THERE WAS NOISE OVERSENSING WHEN THE PATIENT COUGHED. A LEAD FRACTURE WAS SUSPECTED. NO PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THIS EVENT. IT WAS FURTHER REPORTED THE LEAD WAS REPLACED.

Description of Event or Problem · 1

IT WAS REPORTED THE LEAD IMPEDANCE VARIED FROM 400 TO 1200 OHMS. IT WAS ALSO REPORTED THAT DURING INTERROGATION, THERE WAS NOISE OVERSENSING WHEN THE PATIENT COUGHED. A LEAD FRACTURE WAS SUSPECTED. 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 IMPLANTABLE TACHY LEAD LWS MEDTRONIC PUERTO RICO, INC. 6947 ASKU

Patients

Seq Age Sex Outcome Treatment
1 81 YR Required Intervention