Recall Z-1972-2025— BD SWITZERLAND SARL
Class II · Ongoing
Class II FDA medical device recall by BD SWITZERLAND SARL, initiated 2025-05-12. FDA's recall record names no specific 510(k) clearance for this event. Product: BD Texium: 3 mL, REF: MY8003-0006; 5 mL, REF: MY8005-0006; 10 mL, REF: MY8010-0006; 20 mL, REF: MY8020-0006; 30 mL, REF: MY8030-0006; 60 mL, REF: MY8060-0006. Reason: Sterile, single use closed system drug transfer devices, standalone or on infusion sets or bonded syringes, may leak at the interface between the closed male luer component and the needle-free connector, which may cause procedure delay, treatment interruptions, exposure to hazardous drugs, and/or underdosing of medication..
- Recalling firm
- BD SWITZERLAND SARL
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-05-12
- Firm location
- Eysins, Switzerland
Product description
BD Texium: 3 mL, REF: MY8003-0006; 5 mL, REF: MY8005-0006; 10 mL, REF: MY8010-0006; 20 mL, REF: MY8020-0006; 30 mL, REF: MY8030-0006; 60 mL, REF: MY8060-0006
Reason for recall
Sterile, single use closed system drug transfer devices, standalone or on infusion sets or bonded syringes, may leak at the interface between the closed male luer component and the needle-free connector, which may cause procedure delay, treatment interruptions, exposure to hazardous drugs, and/or underdosing of medication.
Data sourced from openFDA. This site is unofficial and independent of the FDA.