MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION QUANTUM MAVERICK; CATHETERS, TRANSLUMINAL CORONARY ANGIOPLASTY, PERCUTANEOUS

Model Number	7005
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	08/20/2018
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that shaft break occurred.A 3.0mm x 8mm quantum maverick balloon catheter was selected for dilatation.However, it was noted that the balloon delivery shaft got fractured.The procedure was completed with a different device.No patient's complications were reported and the patient status was stable.
Event or Problem Description
It was reported that shaft break occurred.A 3.0mm x 8mm quantum maverick balloon catheter was selected for dilatation.However, it was noted that the balloon delivery shaft got fractured.The procedure was completed with a different device.No patient's complications were reported and the patient status was stable.Device evaluated by mfr: the outer shaft, inner shaft, balloon and tip were visually and microscopically examined.Visual examination revealed that the hypotube is separated 81.2cm from the hub.There are multiple kinks along the whole device.Microscopic examination did not reveal any damages.There is blood present in the inflation lumen and in the guidewire lumen.Inspection of the remainder of the device presented no other damage or irregularities.Product analysis confirmed the shaft is separated and appeared to be kinked prior to separation.

• Brand Name: QUANTUM MAVERICK
• Common Device Name: CATHETERS, TRANSLUMINAL CORONARY ANGIOPLASTY, PERCUTANEOUS
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; two scimed place; maple grove MN 55311
• MDR Report Key: 7886945
• Report Number: 2134265-2018-61084
• Device Sequence Number: 1985950
• Product Code: LOX
• UDI-Device Identifier: 08714729392569
• UDI-Public: 08714729392569
• Combination Product (Y/N): N
• Initial Reporter Country: CH
• PMA/510(K) Number: P860019
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,distri
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 10/22/2018

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: 06/12/2021
• Device Model Number: 7005
• Device Catalogue Number: 7005
• Device Lot Number: 0022244654
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 09/18/2018
• Initial Date Received by Manufacturer: 08/24/2018
• Supplement Date Received by Manufacturer: 09/27/2018
• Initial Report FDA Received Date: 09/18/2018
• Supplement Report FDA Received Date: 10/22/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1