MAUDE Adverse Event Report: BD (SUZHOU) BD INTIMA-II CLOSED IV CATHETER SYSTEM; INTRAVASCULAR CATHETER

Catalog Number 383033

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problems Extravasation (1842); Pain (1994); Swelling (2091)

Event Date 10/22/2020

Event Type  Injury  

Manufacturer Narrative

A device evaluation is anticipated but has not yet begun.Upon completion of the investigation, a supplemental report will be filed.(b)(4).

Event Description

It was reported that the bd intima-ii¿ closed iv catheter system caused extravasation in the patient, and a "magnesium sulfate wet hot compress" was used on the "red parts" of the patient's affected area.The following information was provided by the initial reporter, translated from (b)(6) to english: "on (b)(6), 2020 patients with coronary heart disease (chd) in undergraduate course, in no.20002087 , because of illness need to closed venous indwelling needle puncture infusion, at 15:12 the patient reported redness, swelling and pain around the indwelling needle, nurse examined and revealed needle push drug resistance, fluid extravasation, pull, prescribed for red parts of magnesium sulfate wet hot compress, change the body to continue to infusion.The patient's transfusion was normal.On (b)(6), the patient's coronary heart disease improved and left the hospital, and the limbs partially returned to normal.".

Manufacturer Narrative

H.6.Investigation: a device history review was conducted for lot number 0063924.Our records show that this is the only instance of this issue occurring in this production batch.According to the sampling plan applied for product performance, this lot was accepted and released without defects being noted during the final assembly or visual inspections.A sample could not be obtained for evaluation and testing; in lieu of the affected device, functional testing was performed on retention samples for this lot, the results of these show that the tested units performed within product specifications.Unfortunately without the ability to investigate the affected unit our quality engineers were unable to determine the root cause for this the reported functional non-conformance.Additionally, this lot was treated and received a certificate of conformance for sterility.H3 other text : see h.10.

Event Description

It was reported that the bd intima-ii¿ closed iv catheter system caused extravasation in the patient, and a "magnesium sulfate wet hot compress" was used on the "red parts" of the patient's affected area.The following information was provided by the initial reporter, translated from chinese to english: "on (b)(6) 2020 patients with coronary heart disease (chd) in undergraduate course, in no.(b)(4), because of illness need to closed venous indwelling needle puncture infusion, at 15:12 the patient reported redness, swelling and pain around the indwelling needle, nurse examined and revealed needle push drug resistance, fluid extravasation, pull, prescribed for red parts of magnesium sulfate wet hot compress, change the body to continue to infusion.The patient's transfusion was normal.On (b)(6), the patient's coronary heart disease improved and left the hospital, and the limbs partially returned to normal.".

• Brand Name: BD INTIMA-II CLOSED IV CATHETER SYSTEM
• Type of Device: INTRAVASCULAR CATHETER
• Manufacturer (Section D): BD (SUZHOU); no. 5 baiyu road; suzhou industrial park; suzhou
• MDR Report Key: 10939341
• MDR Text Key: 219321745
• Report Number: 3006948883-2020-00881
• Device Sequence Number: 1
• Product Code: FOZ
• Combination Product (y/n): N
• PMA/PMN Number: NA
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: foreign,other,user facility
• Type of Report: Initial,Followup
• Report Date: 01/27/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Expiration Date: 03/30/2023
• Device Catalogue Number: 383033
• Device Lot Number: 0063924
• Was Device Available for Evaluation?: No
• Initial Date Manufacturer Received: 11/06/2020
• Initial Date FDA Received: 12/03/2020
• Supplement Dates Manufacturer Received: 01/27/2021
• Supplement Dates FDA Received: 01/31/2021
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention