MAUDE Adverse Event Report: GUIDANT CRM CLONMEL IRELAND MOMENTUM; IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

Model Number G138

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problems Bacterial Infection (1735); Dyspnea (1816); Fatigue (1849); Fever (1858); Patient Problem/Medical Problem (2688)

Event Date 05/30/2018

Event Type  Injury  

Manufacturer Narrative

As no further information concerning this report is expected, our investigation is complete.This investigation will be updated should further information be provided.

Event Description

Boston scientific received information that this patient experienced fatigue, loss of appetite, night sweats, shortness of breath and fever.The patient was hospitalized and a physician determined the reported symptoms were likely related to the patient's chronic kidney disease.Nevertheless, blood cultures revealed the patient suffered an enterococcus infection.As result, antimicrobial treatment and antibiotics were prescribed.This cardiac resynchronization therapy defibrillator (crt-d) was part of the implanted system at the time of the infection.The device remains in service.There were no additional adverse effects reported.

• Brand Name: MOMENTUM
• Type of Device: IMPLANTABLE CARDIOVERTER DEFIBRILLATOR
• Manufacturer (Section D): GUIDANT CRM CLONMEL IRELAND; guidant ireland; clonmel, tipperary ireland
• Manufacturer (Section G): GUIDANT CRM CLONMEL IRELAND; guidant ireland; clonmel, tipperary ireland
• Manufacturer Contact: tim degroot ; 4100 hamline ave. n; st. paul, MN ; 6515826168
• MDR Report Key: 7730653
• MDR Text Key: 115347228
• Report Number: 2124215-2018-14060
• Device Sequence Number: 1
• Product Code: NIK
• UDI-Device Identifier: 00802526589188
• UDI-Public: 00802526589188
• Combination Product (y/n): N
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: consumer
• Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date: 06/19/2018

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 07/30/2018
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Lay User/Patient
• Device Expiration Date: 10/04/2019
• Device Model Number: G138
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: Yes
• Date Manufacturer Received: 06/19/2018
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 10/04/2017
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Treatment: 0185; 4087; 4677; E143; G138; T127
• Patient Outcome(s): Hospitalization; Life Threatening; Required Intervention
• Patient Age: 83 YR