MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION SYNERGY; CORONARY DRUG-ELUTING STENT

Model Number 10623

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

Patient Problems Angina (1710); Heart Failure/Congestive Heart Failure (4446)

Event Date 09/04/2023

Event Type  Injury  

Event Description

Synergy china registry it was reported that left heart failure occurred.In november 2022, the subject presented with myocardial infarction and referred for cardiac catheterization.The target lesion was located in proximal right coronary artery (rca) with 99% stenosis was 36 mm long and a reference vessel diameter of 2.5 mm.The target lesion was treated with pre-dilation and followed by the placement of 2.50 mm x 38 mm synergy stent system.Following post dilation, residual stenosis was noted to be 0%.Twelve days later, the subject was discharged on aspirin and clopidogrel.In september 2023, the subject was diagnosed with stable angina pectoris, left heart failure and was hospitalized on the same day for further treatment.Medication was given to treat the event.Nine days later, the event was considered to be recovered/resolved and the subject was discharged with aspirin and clopidogrel.

• Brand Name: SYNERGY
• Type of Device: CORONARY DRUG-ELUTING STENT
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; 300 boston scientific way; marlborough MA 01752
• Manufacturer (Section G): BOSTON SCIENTIFIC CORPORATION; ballybrit business park; galway ; EI
• Manufacturer Contact: rachel shields ; 4100 hamline ave n; arden hills, MN 55112 ; 6512422111
• MDR Report Key: 18536571
• MDR Text Key: 333155000
• Report Number: 2124215-2023-75017
• Device Sequence Number: 1
• Product Code: NIQ
• Combination Product (y/n): Y
• Reporter Country Code: CH
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Other,Foreign,Study,Health Professional,Company Representative
• Reporter Occupation: Physician
• Type of Report: Initial
• Report Date: 01/18/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 01/18/2024
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Expiration Date: 01/05/2024
• Device Model Number: 10623
• Device Catalogue Number: 10623
• Device Lot Number: 0028650344
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 12/26/2023
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 01/05/2022
• 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
• Patient Outcome(s): Hospitalization; Required Intervention
• Patient Age: 63 YR
• Patient Sex: Male