Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD Texium: 3 mL Recalled by BD SWITZERLAND SARL Due to Sterile, single use closed system drug transfer devices,...
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 BD SWITZERLAND SARL directly.
Affected Products
BD Texium: 3 mL, REF: MY8003-0006; 5 mL, REF: MY8005-0006; 10 mL, REF: MY8010-0006; 20 mL, REF: MY8020-0006; 30 mL, REF: MY8030-0006; 60 mL, REF: MY8060-0006
Quantity: 812,165
Why Was This Recalled?
Sterile, single use closed system drug transfer devices, standalone or on infusion sets or bonded syringes, may leak at the interface between the closed male luer component and the needle-free connector, which may cause procedure delay, treatment interruptions, exposure to hazardous drugs, and/or underdosing of medication.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About BD SWITZERLAND SARL
BD SWITZERLAND SARL has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report