MAUDE Adverse Event Report: VOLCANO CORPORATION VISIONS PV .014 P RAPID EXCHANGE DIGITAL IVUS CATHETER; CATHETER, ULTRASOUND, INTRAVASCULAR

Model Number	85910P
Medical Device Problem Code	Material Separation (1562)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	07/02/2018
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(6).Attempts to obtain patient information have been unsuccessful.Facility declined to provide the information.No tests/laboratory data was available.The implant or explant dates are not applicable to this device.
Event or Problem Description
This case was reviewed and investigated according to the manufacturer's policy.It was reported the image disappeared on the manufacturer's device.A second of the same make and model of the manufacturer's device was used to successfully complete the procedure.There was no patient injury and no adverse events.Visual, microscopic inspection and functional testing were performed on the returned device.The adhesive at the distal fillet was lifted and a portion of the adhesive was missing.The device was recognized by the system and produced a proper image during image testing.No error was observed with manipulation near the scanner body.The probable cause of the reported "image disappeared" failure is an insufficient amount of adhesive that led to fluid ingress and electrical discontinuity at the scanner body as a result.The probable cause of the observed portion of missing adhesive could not be conclusively determined by the investigation, and therefore it could not be determined when the cause of the failure occurred.Strain, impact, and forces associated with use can affect the integrity of the device.The manufacturing documentation for this device was reviewed and the device met all quality and manufacturing release criteria.This event is being reported as there is a potential for harm if the malfunction were to recur.
Event or Problem Description
This follow-up supplemental report #1 is being submitted to correct date of report.
Additional Manufacturer Narrative
Internal reference: 215566 this case was reviewed and investigated according to the manufacturer's policy.Block b4: inadvertent entry error.Submission of this report does not, in itself, represent a conclusion by the manufacturer and/or authorized representative or the national competent authority that the content of this report is complete or accurate, that the medical device(s) listed failed in any manner and/or that the medical device(s) caused or contributed to the alleged death or deterioration in the state of the health of any person.
Event or Problem Description
This case was reviewed and investigated according to the manufacturer''s policy.Internal reference: (b)(4).This follow-up supplemental report #2 is being submitted to report additional investigation findings, to wit: there is no potential for harm if the malfunction were to recur.This complaint was reassessed based on an engineering study that indicated, this family of catheters do not exhibit any adhesive detachment during normal use.There is no evidence of abnormal use conditions, it is likely the adhesive detached post-procedure, during the process of returning the device for analysis.There was no patient injury, no status decline, no adverse event, and no unplanned additional medical or surgical intervention reported.There is no potential for harm if the malfunction were to recur.Submission of this report does not, in itself, represent a conclusion by the manufacturer and/or authorized representative or the national competent authority that the content of this report is complete or accurate, that the medical device(s) listed failed in any manner and/or that the medical device(s) caused or contributed to the alleged death or deterioration in the state of the health of any person.
Additional Manufacturer Narrative
H3 other text : placeholder.
Additional Manufacturer Narrative
Block h6: supplemental report #2 indicated that the adhesive likely detached post procedure; however, the conclusion code was not updated from 4307 (cause traced to component failure) to 4308 (cause traced to transport/storage).

• Brand Name: VISIONS PV .014 P RAPID EXCHANGE DIGITAL IVUS CATHETER
• Common Device Name: CATHETER, ULTRASOUND, INTRAVASCULAR
• Manufacturer (Section D): VOLCANO CORPORATION; 2870 kilgore road; rancho cordova CA 95670
• Manufacturer (Section G): VOLCARICA S.R.L.; coyol free zone&business park; alajuela, B37 ; CS B37
• Manufacturer Contact: melissa pieplow ; 2870 kilgore road; rancho cordova, CA 95670 ; 9163651925
• MDR Report Key: 7815540
• Report Number: 2939520-2018-00086
• Device Sequence Number: 16437965
• Product Code: OBJ
• UDI-Device Identifier: 00845225002428
• UDI-Public: (01)00845225002428(17)200531(10)0301446217(90)989609000951
• Combination Product (Y/N): Y
• Initial Reporter Country: JA
• PMA/510(K) Number: K143701
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup,Followup
• Report Date (Section B): 07/02/2018
• Report Date (Section F): 01/01/2005

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: 05/31/2020
• Device Model Number: 85910P
• Device Catalogue Number: 400-0200.233
• Device Lot Number: 0301446217
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 07/26/2018
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Date Report to Manufacturer: 01/10/2005
• Initial Date Received by Manufacturer: 07/26/2018
• Supplement Date Received by Manufacturer: 04/18/2019; 01/14/2005; 12/13/2021
• Initial Report FDA Received Date: 08/27/2018
• Supplement Report FDA Received Date: 04/19/2019; 03/04/2020; 12/30/2021
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 05/04/2018
• 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 Sex: Unknown
• Date Report Sent to FDA: 01/01/2005