Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD Nexiva Closed IV Catheter System - Single Port REF Recalled by Becton Dickinson Infusion Therapy Systems Inc. Due to During needle withdrawal, the tip shield may prematurely...
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 Infusion Therapy Systems Inc. directly.
Affected Products
BD Nexiva Closed IV Catheter System - Single Port REF 383516 20 GA X1.0o in (1.1 x 25 mm) 61 mL/min (3660 mL/hr)
Quantity: 56,080 units
Why Was This Recalled?
During needle withdrawal, the tip shield may prematurely separate from the catheter adapter and preventing the needle tip from being in the safely shielded (leaving the needle tip exposed).
Where Was This Sold?
U.S.: New York, Florida, Maryland, North Carolina, Virginia, Georgia, Rhode Island, New Jersey, Pennsylvania, Illinois, South Carolina, Maine, and Massachusetts. O.U.S.: N/A
About Becton Dickinson Infusion Therapy Systems Inc.
Becton Dickinson Infusion Therapy Systems Inc. has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report