MAUDE Adverse Event Report: COOK INC NEFF PERCUTANEOUS ACCESS SET; KGZ ACCESSORIES, CATHETER

Model Number N/A

Device Problems Material Separation (1562); Unraveled Material (1664)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Date 06/01/2022

Event Type  malfunction  

Event Description

It was reported that the wire guide in a neff percutaneous access set unraveled.During a drainage procedure, the wire guide was advanced through the needle but became damaged and unraveled; no portion of the device was retained in the patient.A new device was opened to complete the procedure.It was noted that it is unknown if the wire guide was removed through a needle or other instrument; however, resistance was encountered during removal.The device was stored vertically and no damage to the package was observed.As reported, the patient did not experience any adverse effects or require any additional procedures due to this occurrence.

Manufacturer Narrative

Blank fields on this form indicate the information is unknown or unavailable.E1 - customer (person): (b)(6).G4 ¿ pma/510(k) #: exempt.This report includes information known at this time.A follow-up report will be submitted should additional, relevant information become available.This report is required by the fda under 21 cfr part 803 and is based on unconfirmed information submitted by others.Neither the submission of this report nor any statement contained herein is intended to be an admission that any cook device is defective or malfunctioned or that a death or serious injury occurred; nor is it admission that any cook device caused, contributed to, or is likely to cause or contribute to a death or serious injury if a malfunction occurred.

Event Description

Per preliminary device failure analysis of the returned complaint device on 08may2023, the wire guide was confirmed to be stretched and elongated.Additionally, the mandrill (inner wire) of the wire guide was noted to be separated.

Manufacturer Narrative

This report includes information known at this time.A follow-up report will be submitted should additional, relevant information become available.This report is required by the fda under 21 cfr part 803 and is based on unconfirmed information submitted by others.Neither the submission of this report nor any statement contained herein is intended to be an admission that any cook device is defective or malfunctioned or that a death or serious injury occurred; nor is it admission that any cook device caused, contributed to, or is likely to cause or contribute to a death or serious injury if a malfunction occurred.

Manufacturer Narrative

Investigation ¿ evaluation.On (b)(6) 2023, (b)(6) hospital (japan) reported an event involving a neff percutaneous access set (rpn: npas-105-rh-nt-u, lot: 14533658).During a drainage procedure on (b)(6) 2022, the customer inserted the wire guide into the puncture needle, in which the wire guide became unraveled.It is not known if any resistance was noted during removal or insertion.It is not known if the wire guide was withdrawn or manipulated through the needle.No part of the device remained within the patient.The patient did not experience any adverse effects due to this occurrence.Reviews of the documentation, including the complaint history, device history record and quality control procedures, as well as a visual inspection of the returned device, were conducted during the investigation.One used device was received for evaluation.The wire guide was found to be stretched and elongated, and it appeared that the inner wire (mandril) was separated.The outer diameter of the undamaged portion of the wire guide was measured and found to be manufactured within specification.Additionally, a document-based investigation evaluation was performed.A review of the device master record (dmr) identified process steps to ensure that nonconforming material does not leave the house.A review of the device history record (dhr) for lot 14533658 and the related subassembly lots found one relevant nonconformance from a component lot, in which three devices were scrapped prior to further processing.It should be noted that there were no other complaints associated with the final product lot number.Cook was not able to review product labeling.This product is not supplied with an instructions for use (ifu) pamphlet.The wire guide holder is supplied with labeling (l_scor) indicating to not withdraw or manipulate the wire guide through a needle.Evidence gathered upon review of the dmr, dhr, and returned device suggests that the device was not manufactured out of specification, and that there are no nonconforming devices in house or out in the field.Based on the information provided, examination of the returned product, and the results of our investigation, a definitive cause for the failure could not be established.The appropriate personnel have been notified.Per the risk assessment no further action is required.Cook will continue to monitor for similar complaints.This report is required by the fda under 21 cfr part 803 and is based on unconfirmed information submitted by others.Neither the submission of this report nor any statement contained herein is intended to be an admission that any cook device is defective or malfunctioned, that a death or serious injury occurred, nor that any cook device caused, contributed to, or is likely to cause or contribute to a death or serious injury if a malfunction occurred.

Event Description

No additional information regarding patient and/or event details has been received since the previous medwatch report was sent.

• Brand Name: NEFF PERCUTANEOUS ACCESS SET
• Type of Device: KGZ ACCESSORIES, CATHETER
• Manufacturer (Section D): COOK INC; 750 daniels way; bloomington IN 47404
• Manufacturer (Section G): COOK INC; 750 daniels way; bloomington IN 47404
• Manufacturer Contact: jason crouch ; 750 daniels way; bloomington, IN 47404 ; 8123392235
• MDR Report Key: 16825960
• MDR Text Key: 314120528
• Report Number: 1820334-2023-00518
• Device Sequence Number: 1
• Product Code: KGZ
• UDI-Device Identifier: 00827002107977
• UDI-Public: (01)00827002107977(17)250211(10)14533658
• Combination Product (y/n): N
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Other,Foreign,User Facility
• Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date: 08/23/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 04/27/2023
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: N/A
• Device Catalogue Number: NPAS-105-RH-NT-U
• Device Lot Number: 14533658
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 08/15/2023
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 02/11/2022
• 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