# FDA device recall: BD Connecta" BD Luer-Lok" 360 REF 394910  UDI-DI code: 00382903949106    BD Connecta" Stopcocks are used to administer f

> recall · VERIFIED · 2026-05-21

Firm: BD SWITZERLAND SARL · Class II · 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 u

- Company: BD SWITZERLAND SARL
- Sector: medtech
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.