# FDA recall Z-1509-2025

> **BD SWITZERLAND SARL** · Class II · device recall initiated 2025-02-20.

## Product

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.

## Reason for recall

Due to specific lots of luer-lok devices were shipped to the U.S. market with an Outside US Instruction for Use (IFU)

## Distribution

U.S.: AK, AL, AR, AZ, CA, CO, FL, GA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NM, NV, OH, OK, OR, PA, SC, TN. TX, UT, VA, WA, WV  O.U.S.: N/A

## Key facts

- **Recall number:** Z-1509-2025
- **Recalling firm:** BD SWITZERLAND SARL
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-02-20
- **Report date:** 2025-04-09

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1509-2025

## Citation

> AI Analytics. FDA recall Z-1509-2025. Retrieved 2026-07-19 from https://api.ai-analytics.org/recall/Z-1509-2025. Source: US FDA. Licensed CC0.

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