MAUDE Adverse Event Report: COOK INC TURBO-JECT POWER INJECTABLE; LJS TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER

Model Number G56194

Device Problem Device Operates Differently Than Expected (2913)

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

Event Date 06/14/2018

Event Type  malfunction  

Manufacturer Narrative

(b)(4).Pma/510(k) #: k111244.This report includes information known at this time.A follow up report will be submitted should additional relevant information become available.

Event Description

It was reported the wire would not pull our of the catheter after a turbo-ject power injectable picc line was inserted.The patient was said to have angulated and tortuous vessels.Another similar device was used to complete the procedure successfully.As reported, the patient did not experience any adverse effects or require any additional procedures due to this occurrence.

Event Description

See h10.

Manufacturer Narrative

Blank fields on this form indicate the information has previously been reported, is unknown or is unavailable.The complaint device was returned on (b)(6) 2018 and evaluated on (b)(6) 2018.The investigation was completed on (b)(6) 2018 and reviewed on (b)(6) 2018.The returned used device met specification and did not show signs of fraying, unraveling, or fragmentation/separation.This complaint no longer meets the fda 21 cfr part 803 definition of a device malfunction.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.

• Brand Name: TURBO-JECT POWER INJECTABLE
• Type of Device: LJS TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER
• Manufacturer (Section D): COOK INC; 750 daniels way; bloomington IN 47404
• MDR Report Key: 7659287
• MDR Text Key: 113192152
• Report Number: 1820334-2018-01900
• Device Sequence Number: 1
• Product Code: LJS
• UDI-Device Identifier: 00827002561946
• UDI-Public: (01)00827002561946(17)200223(10)8616147
• Combination Product (y/n): N
• PMA/PMN Number: K111244
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,foreig
• Type of Report: Initial,Followup
• Report Date: 10/16/2018

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 07/03/2018
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Expiration Date: 02/23/2020
• Device Model Number: G56194
• Device Catalogue Number: UPICDS-5.0-CT-OTW-ST-1110
• Device Lot Number: 8616147
• Was Device Available for Evaluation?: Yes
• Event Location: Hospital
• Date Manufacturer Received: 10/05/2018
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1