MAUDE Adverse Event Report: COOK INC MICROPUNCTURE ACCESS SET; DYB INTRODUCER, CATHETER

Catalog Number MPIS-401-U

Device Problems Kinked (1339); Stretched (1601); Difficult to Advance (2920)

Patient Problem No Known Impact Or Consequence To Patient (2692)

Event Date 05/25/2016

Event Type  malfunction  

Manufacturer Narrative

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 Description

It was reported that after puncture, the wire guide was difficult to advance into the needle.Therefore, it was removed from the patient's body.It was confirmed that the wire guide was stretched and kinked.As a result, another device was used to complete the procedure.There are no known adverse effects to the patient reported as a result of this issue.

• Brand Name: MICROPUNCTURE ACCESS SET
• Type of Device: DYB INTRODUCER, CATHETER
• Manufacturer (Section D): COOK INC; 750 daniels way; bloomington IN 47404
• Manufacturer Contact: larry pool ; 750 daniels way; bloomington, IN 47404 ; 8128294891
• MDR Report Key: 6737295
• MDR Text Key: 81052119
• Report Number: 1820334-2017-01937
• Device Sequence Number: 1
• Product Code: DYB
• UDI-Device Identifier: 00827002074101
• UDI-Public: (01)00827002074101(17)170910(10)5272800
• Combination Product (y/n): N
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: foreign,health professional,u
• Reporter Occupation: Physician
• Type of Report: Initial
• Report Date: 07/24/2017

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
• Device Operator: Health Professional
• Device Catalogue Number: MPIS-401-U
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Initial Date Manufacturer Received: 07/11/2017
• Initial Date FDA Received: 07/24/2017
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 09/10/2014
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1