MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION MACH1; CATHETER, PERCUTANEOUS

Model Number	M001198380
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	11/29/2023
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that a catheter break occurred.A mach1 guide catheter was selected for use.During the procedure, the distal 2-3cm of the catheter was broken and the device did not pass upward to the left common carotid artery.The device was then replaced with another guide catheter which passed smoothly and completed the procedure.No patient complications were reported.
Event or Problem Description
It was reported that a catheter break occurred.A mach1 guide catheter was selected for use.During the procedure, the distal 2-3cm of the catheter was broken and the device did not pass upward to the left common carotid artery.The device was then replaced with another guide catheter which passed smoothly and completed the procedure.No patient complications were reported.It was further reported that the target lesion was non-calcified.The device was removed safely, and the patient condition post procedure was normal.
Additional Manufacturer Narrative
This report is being filed to correct the model number and unique identifier (udi) # in response to an fda request.
Event or Problem Description
It was reported that a catheter break occurred.A mach1 guide catheter was selected for use.During the procedure, the distal 2-3cm of the catheter was broken and the device did not pass upward to the left common carotid artery.The device was then replaced with another guide catheter which passed smoothly and completed the procedure.No patient complications were reported.It was further reported that the target lesion was non-calcified.The device was removed safely, and the patient condition post procedure was normal.

• Brand Name: MACH1
• Common Device Name: CATHETER, PERCUTANEOUS
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; 300 boston scientific way; marlborough MA 01752
• Manufacturer (Section G): FLEXTRONICS INTERNATIONL EUROPE B V; 6201 america center drive; san jose CA 95002
• Manufacturer Contact: rachel shields ; 4100 hamline ave n; arden hills, MN 55112 ; 6512422111
• MDR Report Key: 18364621
• Report Number: 2124215-2023-70728
• Device Sequence Number: 8108596
• Product Code: DQY
• UDI-Device Identifier: 08714729481591
• UDI-Public: (01)08714729481591(17)240828(10)60317091
• Combination Product (Y/N): N
• Initial Reporter Country: EG
• PMA/510(K) Number: K020028
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Other,Health Professional,Company Representative,Distributor
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 07/03/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 08/28/2024
• Device Model Number: M001198380
• Device Catalogue Number: 24974
• Device Lot Number: 0060317091
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 12/05/2023
• Supplement Date Received by Manufacturer: 12/24/2023; 06/12/2024
• Initial Report FDA Received Date: 12/20/2023
• Supplement Report FDA Received Date: 01/09/2024; 07/03/2024
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 08/28/2021
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Age: 80 YR
• Patient Sex: Female
• Patient Weight: 98 KG