FDA Adverse Event Malfunction Summary report: N

SELUTE PICOTIP

MDR report key: 3053240 · Received April 11, 2013

Report

Report Number
2124215-2013-05452
Event Type
Malfunction
Date Received
April 11, 2013
Date of Event
March 20, 2013
Report Date
March 20, 2013
Manufacturer
CPI - DEL CARIBE
Product Code
NVN
PMA / PMN Number
P950001
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

NO FURTHER COMMUNICATION HAS BEEN RECEIVED REGARDING THIS ISSUE. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE, THIS REPORT WILL BE UPDATED.

Description of Event or Problem · 1

BOSTON SCIENTIFIC RECEIVED INFORMATION WHEN THIS PHYSICIAN CONTACTED BOSTON SCIENTIFIC TECHNICAL SERVICES (TS) REQUESTING REVIEW OF A 12 LEAD EKG RHYTHM STRIP. THE VISUAL QUALITY OF THE EKG STRIP WAS POOR, HOWEVER THERE APPEARED TO BE ISSUES WITH NON-CAPTURE/NON-SENSING AT A RATE AROUND 90PPM/680MS. WHEN THE PATIENT WAS CHECKED LATER THAT NIGHT, THE DEVICE FUNCTION APPEARED NORMAL. THEN OVERNIGHT, THE SAME LOSS OF CAPTURE WAS OBSERVED AGAIN. THE PHYSICIAN WAS ON HIS WAY TO EVALUATE THE PATIENT AND STATED HE WOULD CONTACT TS AGAIN WITH FURTHER DETAILS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
156853 SELUTE PICOTIP IMPLANTABLE LEAD NVN CPI - DEL CARIBE 4034

Patients

Seq Age Sex Outcome Treatment
1 79 YR 1290| 1283| 4086| 4034