BD recalls Alaris Pump Infusion Sets with SmartSite bags that may leak at connections, risking treatment delays or medication underdosing. Check product references listed.
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 Alaris Pump Infusion Sets with SmartSite bags because they may leak at the connection point between the bag and needle-free connector. This could lead to treatment interruptions, exposure to hazardous drugs, or underdosing of medication.
The closed system drug transfer devices may leak at the interface between the closed male luer component and the needle-free connector. This leak can cause procedure delays, treatment interruptions, exposure to hazardous drugs, or underdosing of medication.
Healthcare professionals using these specific infusion sets for medication delivery are most at risk. Patients receiving treatment through these devices may experience delays or incorrect dosing.
Check for product references listed in the recall: 10013361T, 10321213T, 22000-B007T, 22600-0007T, 22602-B007T, 22603-B007T, 24010-0007T, 24301-0007T, 24601-B007T, 70001B-07T, 20350ET, 40000-07T, 10013364T, 4030B-07T, 22005E-07T.
Look for the product reference codes listed in the recall (e.g., 10013361T, 10321213T) on the packaging or label.
The Alaris Pump Infusion Sets with SmartSite bags may leak at the interface between the closed male luer component and the needle-free connector, which can cause treatment delays, medication underdosing, or exposure to hazardous drugs.
The recall does not specify a remedy; check the product references listed to see if your item is affected. If affected, contact BD for further instructions.
Check the product reference code on the packaging or label against the list provided in the recall: 10013361T, 10321213T, 22000-B007T, 22600-0007T, 22602-B007T, 22603-B007T, 24010-0007T, 24301-0007T, 24601-B007T, 70001B-07T, 20350ET, 40000-07T, 10013364T, 4030B-07T, 22005E-07T.
We’ve drafted a message you can send BD to request your refund or repair — edit it as you like.
Subject: Recall Z-1970-2025 — BD BD Hello, I own a BD that is covered by recall Z-1970-2025 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.
