BD recalls Luer-Lok 360 stopcocks with UDI-DI code 00382903949106 due to potential overthreading causing unstable connections during IV fluid administration.
Due to stopcock issues when using the plastic luer-lok syringe, the connection at the Port C may over thread or continue to spin rather than tightening securely. This behavior has led some clinical users to perceive the connection as unstable.
BD is recalling Luer-Lok 360 stopcocks that may overthread or spin when connecting to IV lines, which could lead to unstable connections. This poses a risk of leaks or disconnections during medical use, potentially causing medication errors or delays in treatment.
The stopcock's connection at Port C may overthread or continue spinning instead of tightening securely. This instability can cause the connection to become loose during use, potentially leading to leaks or disconnections of IV lines. Such issues could result in medication errors or delays in treatment.
Healthcare professionals using these stopcocks for IV fluid administration are most at risk. Patients receiving IV treatments with these devices could experience complications if connections become unstable.
Check for the UDI-DI code 00382903949106 on the stopcock packaging or label. The product is identified by the model number 394910 and lot numbers listed in the recall notice.
Verify the model number 394910 and UDI-DI code 00382903949106 on the stopcock packaging or label.
Reach out to BD directly for a replacement stopcock if you have the recalled model.
The stopcock may overthread or continue spinning instead of tightening securely, causing unstable connections during IV use.
The UDI-DI code is 00382903949106.
Check for the model number 394910 and UDI-DI code 00382903949106 on the stopcock packaging or label.
We’ve drafted a message you can send BD to request your refund or repair — edit it as you like.
Subject: Recall Z-2514-2026 — BD BD Hello, I own a BD that is covered by recall Z-2514-2026 from BD. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
