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 Problem Angina (1710)

Event Date 08/20/2023

Event Type  Injury  

Event Description

\synergy china registry it was reported that angina occurred.In march 2020, the subject was referred for cardiac catheterization.The target lesion was located in the middle right coronary artery (rca) extending up to distal rca with 99% stenosis and was 71 mm long with a reference vessel diameter of 2.76 mm.The target lesion was treated with pre-dilatation and placement of 2.50 mm x 38 mm and 2.75 mm x 38 mm synergy stent systems.Following post-dilatation, the residual stenosis was noted to be 0%.The next day, the subject was discharged on clopidogrel and other medications.In august 2023, the subject was diagnosed with stable angina pectoris and the subject was hospitalized for further treatment.Medication was given to treat the event.Three days later, the event was considered to be recovered/resolved and the subject was discharged on clopidogrel and other medication.

• 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: 18573911
• MDR Text Key: 333628934
• Report Number: 2124215-2024-01092
• 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: 01/24/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Expiration Date: 07/21/2020
• Device Model Number: 10623
• Device Catalogue Number: 10623
• Device Lot Number: 0023272545
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Initial Date Manufacturer Received: 01/02/2024
• Initial Date FDA Received: 01/24/2024
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 01/23/2019
• 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: 57 YR
• Patient Sex: Male