Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD Q-Syte Luer Access Split Septum Recalled by Becton Dickinson & Company Due to Becton Dickinson received an elevated number of complaints...
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 Q-Syte Luer Access Split Septum, 0.16 ml, Sterile, Rx only, Catalog REF #385100, Manufacturer: Becton Dickinson Infusion Therapy Systems Inc. An accessory to an intravascular administration set that permits injection, gravity flow or withdrawal of fluids.
Quantity: 315,800 units
Why Was This Recalled?
Becton Dickinson received an elevated number of complaints for blood or infusate/medication leakage due to tearing of the silicone septum.
Where Was This Sold?
This product was distributed to 9 states: CA, CT, FL, IL, MA, NY, ND, OH, PA
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