Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System Recalled by Becton Dickinson & Company Due to Leak from the septum assembly or the canister...

Date: March 1, 2019
Company: Becton Dickinson & Company
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Becton Dickinson & Company directly.

Affected Products

BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog Number: 383536

Quantity: 6,720 units

Why Was This Recalled?

Leak from the septum assembly or the canister may burst under high pressure which could result in blood exposure to a health care worker.

Where Was This Sold?

This product was distributed to 1 state: VA

Affected (1 state)Not affected

About Becton Dickinson & Company

Becton Dickinson & Company has 169 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report