Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD Connecta BD Luer-Lok 360 Recalled by BD SWITZERLAND SARL Due to Due to specific lots of luer-lok devices were...
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 Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and 3-way Stopcocks are control valves for use in IV. therapy and hemodynamic pressure monitoring.
Quantity: 500 units
Why Was This Recalled?
Due to specific lots of luer-lok devices were shipped to the U.S. market with an Outside US Instruction for Use (IFU)
Where Was This Sold?
This product was distributed to 35 states: AL, AK, AZ, AR, CA, CO, FL, GA, IL, IN, KS, KY, LA, MD, MA, MI, MN, MS, MO, NE, NV, NJ, NM, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WV
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