Use caution Medical device recall · FDA · Published May 21, 2026

BD Connecta Luer-Lok 360 Stopcocks May Overthread - Recall for IV Use

BD recalls Luer-Lok 360 stopcocks with UDI-DI code 00382903949106 due to potential overthreading causing unstable connections during IV fluid administration.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2514-2026Medical device BD ›

Use caution until it’s fixed

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.

Take action

Contact the company

Recalling firmBD SWITZERLAND SARLTerre Bonne Park A4, Route De Crassier 17 · Eysins, Switzerland

✎ GovInfoNow plain-language explainer

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. Read more at govinfonow.com/recall/49113-bd-connecta-luer-lok-360-stopcocks-may-overthread-recall-for.

Source Summary by GovInfoNow · govinfonow.com/recall/49113-bd-connecta-luer-lok-360-stopcocks-may-overthread-recall-for · Updated August 10, 2026 · FDA enforcement record: FDA #Z-2514-2026

Cite this page

“BD Connecta Luer-Lok 360 Stopcocks May Overthread - Recall for IV Use.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/49113-bd-connecta-luer-lok-360-stopcocks-may-overthread-recall-for. Based on FDA recall #Z-2514-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2514-2026%22&limit=1).

BD SWITZERLAND SARL voluntarily recalled BD Connecta BD Luer-Lok 360 stopcocks due to connection issues that may cause instability, according to the FDA on May 21, 2026.

How to tell if you have it

Brand: BD
Product: BD Connecta BD Luer-Lok 360 REF 394910
UDI-DI code: 00382903949106
Lot Numbers: 4277968, 4277973, 4282451, 4282461, 4289801, 4290582, 4292904, 4295848, 4299949, 4303841, 4305108, 4306700, 5129635, 5129642, 5129649, 5129650, 5129651, 5139250, 5139251, 5139252, 5150181, 5153940, 5164061, 5164062, 5178078, 5181442, 5183810, 5183816, 5183824, 5183828, 5218287, 5218291, 5218293, 5218299, 5218302, 5241476, 5247729, 5247731, 5251098, 5275601, 5275602
Units affected: 2,465,500

The hazard

The FDA stated that stopcock issues when using the plastic luer-lok syringe may cause the connection at Port C to over thread or continue spinning rather than tightening securely. This behavior has led some clinical users to perceive the connection as unstable.

Context

GovInfoNow's records show BD SWITZERLAND SARL has 8 other recalls on record since April 9, 2020. Other recent recalls include a June 16, 2026 recall of BD 60-In Extension Sets for inadequate sterilization and a June 4, 2026 recall of BD MEDLINE 111 Gravity Set with 3 Needle-Free Y-Sites for being not for human use. Similar product recalls include Medline Medical Kits and Medline Medical Convenience Kits on February 27, 2026, both citing risk of syringe connection disconnection.

How to tell if you have this one

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.

Brand
BD
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Stopcock Model
Verify the model number 394910 and UDI-DI code 00382903949106 on the stopcock packaging or label.
Contact BD for Replacement
Reach out to BD directly for a replacement stopcock if you have the recalled model.

Where it went and when

Where it was distributed

Distributed in 38 states and D.C., and outside the U.S.

FDA distribution: “U.S.: AK, AL, AR, AZ, CA, CO, DC, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, and WV. O.U.S.: Japan” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Alaska, Arizona, Arkansas, California, Colorado, District of Columbia, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Nebraska, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin.

Recall timeline

FDA published this recall 34 days after the firm started it.

May 21, 2026Firm started the recall
Jun 18, 2026FDA classified it Class II
Jun 24, 2026Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/49113-bd-connecta-luer-lok-360-stopcocks-may-overthread-recall-for">BD Connecta Luer-Lok 360 Stopcocks May Overthread - Recall for IV Use (GovInfoNow)</a>

Where this comes from

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.

Official source: FDA Recall #Z-2514-2026 (May 21, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2514-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.