CareFusion recalls BD Alaris Pump Infusion Sets with specific reference numbers due to potential flow rate and bolus accuracy issues that could affect patient safety.
Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.
CareFusion is recalling BD Alaris Pump Infusion Sets with certain reference numbers because they may not function correctly, potentially causing incorrect medication delivery. This could lead to unsafe treatment outcomes for patients using these devices.
The infusion sets may not perform within safe limits for flow rate and medication accuracy, which could result in incorrect dosing or treatment interruptions. This poses a risk of improper medication delivery during critical medical procedures.
Patients using BD Alaris Pump Infusion Sets with the listed reference numbers are affected. Those with diabetes or other conditions requiring precise medication delivery are at higher risk.
Check the reference numbers on the packaging: C24101E, 10015414, 2447-0007, 24201-0007, 10012645, 2426-0500, 11522558, 2410-0500, 2232-0007, 11613191, 10012144, 10013034, 10013037, 11582773. These sets were sold with specific lot numbers and UDI codes.
Review the reference numbers and lot codes on the packaging to confirm if your set is affected.
The infusion sets may not perform within safe limits for flow rate and bolus accuracy, which could lead to incorrect medication delivery.
The recall does not specify a remedy, so check the reference numbers and contact CareFusion for further instructions.
Yes, the sets could cause incorrect medication delivery, which may affect patient safety during treatment.
We’ve drafted a message you can send BD Alaris to request your refund or repair — edit it as you like.
Subject: Recall Z-0035-2026 — BD Alaris BD Alaris Hello, I own a BD Alaris that is covered by recall Z-0035-2026 from BD Alaris. 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.
