BD recalls specific needle-free syringes (3mL to 60mL) due to potential leaks at the connection point, which could cause treatment delays, medication underdosing, or exposure to hazardous drugs.
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.
BD is recalling certain needle-free syringes that may leak at the connection point, potentially causing treatment delays, medication underdosing, or exposure to hazardous drugs. This affects specific sizes and batch numbers.
The syringes may leak at the interface between the closed male luer component and the needle-free connector. This leak could lead to procedure delays, treatment interruptions, exposure to hazardous drugs, or underdosing of medication during medical procedures.
Healthcare professionals and patients using the recalled BD Texium Needle-Free Syringes (3mL to 60mL) with the listed reference numbers and expiration dates. Those most at risk are individuals administering medications in clinical settings where leaks could disrupt treatment.
Check the product reference numbers (REF) listed in the recall: MY8003 for 3mL, MY8005 for 5mL, MY8010 for 10mL, MY8020 for 20mL, MY8030 for 30mL, and MY8060 for 60mL. Also check the expiration dates and lot numbers provided in the recall notice.
Identify the reference number (REF) and expiration date on the syringe packaging to confirm if it is in the recalled list.
No, only specific sizes (3mL, 5mL, 10mL, 20mL, 30mL, 60mL) with the listed reference numbers and expiration dates are affected.
Check the reference number (REF) on the syringe packaging. The recalled models have specific REF codes like MY8003 for 3mL, MY8005 for 5mL, and others listed in the recall notice.
The recall does not specify a remedy, so you should check with BD directly for guidance on safe disposal or replacement options.
We’ve drafted a message you can send BD to request your refund or repair — edit it as you like.
Subject: Recall Z-1971-2025 — BD BD Hello, I own a BD that is covered by recall Z-1971-2025 from BD. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
