MAUDE Adverse Event Report: MICROVENTION, INC. SCEPTER C OCCLUSION BALLOON (4X15 MM); OCCLUSION BALLOON CATHETER

Model Number	BC0415C-ID-700
Medical Device Problem Code	Deflation Problem (1149)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	11/11/2020
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
A search for non-conformance associated with this part/lot number combination did not reveal any production-related issues relevant to the complaint that occurred during manufacturing of the device.The device was received by the manufacturer for evaluation.The investigation of the device is underway.
Event or Problem Description
It was reported that the balloon did not correctly deflate during the procedure.There was no reported patient injury or additional intervention.
Additional Manufacturer Narrative
Additional information provided indicated the balloon was used during treatment of an internal carotid artery aneurysm.The balloon was slow to deflate.The balloon was removed from the patient without incident.Investigation of the returned device revealed a pinhole in the balloon, which would have caused the slow deflation; however, the conditions or circumstances that led to the balloon damage could not be determined.

• Brand Name: SCEPTER C OCCLUSION BALLOON (4X15 MM)
• Common Device Name: OCCLUSION BALLOON CATHETER
• Manufacturer (Section D): MICROVENTION, INC.; 35 enterprise drive; aliso viejo CA 92656
• MDR Report Key: 11168473
• Report Number: 2032493-2021-00012
• Device Sequence Number: 14343501
• Product Code: MJN
• UDI-Device Identifier: 00842429103395
• UDI-Public: (01)00842429103395(11)200402(17)230331(10)20040258Y
• Combination Product (Y/N): N
• Initial Reporter Country: FR
• PMA/510(K) Number: K121785
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 02/06/2021

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: Other
• Device Expiration Date: 03/31/2023
• Device Model Number: BC0415C-ID-700
• Device Lot Number: 20040258Y
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 01/08/2021
• Initial Date Received by Manufacturer: 12/14/2020
• Supplement Date Received by Manufacturer: 01/08/2021
• Initial Report FDA Received Date: 01/13/2021
• Supplement Report FDA Received Date: 02/07/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1