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...
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
About Becton Dickinson & Company
Becton Dickinson & Company has 169 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report