# FDA recall Z-2514-2026

> **BD SWITZERLAND SARL** · Class II · device recall initiated 2026-05-21.

## Product

BD Connecta" BD Luer-Lok" 360 REF 394910  UDI-DI code: 00382903949106    BD Connecta" Stopcocks are used to administer fluids or medication through one or two different ports via an IV cannula or extension tube. The ports can be used to sample blood or for hemodynamic monitoring. When used with IV lipid nutritional products, the stopcock device can be used for up to 24 hours.

## Reason for recall

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.

## 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

## Key facts

- **Recall number:** Z-2514-2026
- **Recalling firm:** BD SWITZERLAND SARL
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-21
- **Report date:** 2026-06-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Eysins, Switzerland

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2514-2026

## Citation

> MORVS. FDA recall Z-2514-2026. Retrieved 2026-10-19 from https://api.morvs.ai/recall/Z-2514-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*