FDA Adverse Event Death Summary report: N

ADAPTA DR

MDR report key: 3170958 · Received June 14, 2013

Report

Report Number
3004209178-2013-10409
Event Type
Death
Date Received
June 14, 2013
Date of Event
May 7, 2013
Report Date
July 13, 2013
Manufacturer
MEDTRONIC MED REL MEDTRONIC PUERTO RICO
Product Code
NVZ
PMA / PMN Number
P980035
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

ATTEMPT(S) FOR ADDITIONAL INFORMATION WITH THE PHYSICIAN OFFICE WERE UNSUCCESSFUL. HOWEVER, IF REQUESTED ADDITIONAL INFORMATION IS SUBSEQUENTLY RECEIVED IT WOULD BE PROCESSED AND CONSIDERED ACCORDINGLY. THE DATE OF DEATH IS APPROXIMATE AS THE EXACT DATE IS UNKNOWN. PRODUCT ID: 5076-52, IMPLANTED: (B)(6) 2013; PRODUCT ID: 5076-45, IMPLANTED: (B)(6) 2013. (B)(4).

Additional Manufacturer Narrative · 1

PRODUCT EVENT SUMMARY: (B)(4) THE DEVICE WAS RETURNED AND ANALYZED AND NO ANOMALIES WERE FOUND.

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

A PATIENT WAS REPORTED AS DECEASED WITH LIMITED INFORMATION THE PATIENT RECEIVED AN IMPLANTABLE PULSE GENERATOR (IPG) SYSTEM APPROXIMATELY ONE WEEK PRIOR TO THE DEATH. A CAUSE OF DEATH WAS REQUESTED AND NOT RECEIVED.

Description of Event or Problem · 1

ADDITIONAL INFORMATION WAS RECEIVED FROM THE HOSPITAL'S CORONER REPORT INDICATED THE CAUSE OF DEATH AS AN ACUTE MYOCARDIAL INFARCTION. IT WAS ALSO NOTED THAT THERE WERE ATRIAL SPIKES WITH NO CAPTURE AND VENTRICULAR SPIKES WITH WIDENING QRS COMPLEX AND APPROXIMATELY TWO HOURS LATER, THE PATIENT WAS FOUND PULSELESS AND APNEIC. THE HOSPITAL ALSO INCLUDED THE PATIENT'S PAST MEDICAL HISTORY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
271292 ADAPTA DR PULSE GENERATOR, PERMANENT, IMPLANTABLE NVZ MEDTRONIC MED REL MEDTRONIC PUERTO RICO ADDRS1

Patients

Seq Age Sex Outcome Treatment
1 00068 YR Death