Class II — Potential Health Hazard

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...

Date: February 20, 2025
Company: BD SWITZERLAND SARL
Status: Ongoing
Source: FDA (Device)

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

Affected (35 states)Not affected

About BD SWITZERLAND SARL

BD SWITZERLAND SARL has 11 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report