MAUDE Adverse Event Report: COOK INC ATB ADVANCE BALLOON CATHETER

Catalog Number	ATB5-35-40-12-4.0
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	10/28/2015
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Common device name: dqy.This mdr is being filed after the associated complaint was reviewed under remediation protocol (b)(4), complaint/mdr retrospective review and remediation and reassessed as reportable.Additional complaint investigation and record remediation was not performed.
Event or Problem Description
It was reported that the atb advance balloon catheter could not deflate while being used on a cat.The balloon was punctured with a needle in order to be removed.There were no injuries or additional procedures reported.

• Brand Name: ATB ADVANCE BALLOON CATHETER
• Manufacturer (Section D): COOK INC; 750 daniels way; bloomington IN 47404
• MDR Report Key: 7592186
• Report Number: 1820334-2018-01782
• Device Sequence Number: 16567726
• Product Code: DQY
• UDI-Device Identifier: 00827002441422
• UDI-Public: (01)00827002441422(17)170309(10)5704174
• Combination Product (Y/N): N
• Initial Reporter State: NY
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,user f
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 06/12/2018

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 Catalogue Number: ATB5-35-40-12-4.0
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/06/2018
• Initial Report FDA Received Date: 06/12/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1