BD Alaris Pump Infusion Sets with specific model numbers may not deliver medication at correct flow rates or bolus doses, risking incorrect treatment. Affected units include those with back check valves and SmartSite Y-sites.
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 recalls specific BD Alaris Pump Infusion Sets that may not deliver medication at the correct flow rate or bolus dose, which could lead to incorrect treatment. This affects patients using these pumps for medical infusion therapy.
The infusion pump modules used with these sets may operate outside safe performance ranges for flow rate, bolus accuracy, and occlusion alarms. This could cause medication to be delivered too slowly or too quickly, leading to incorrect treatment.
Patients using BD Alaris Pump Infusion Sets for medical infusion therapy are most at risk. The recall covers specific model numbers and variants sold with back check valves and SmartSite Y-sites.
Check for model numbers like 10013186, 2452-0007, or 2204-0007 on the product packaging. These sets include back check valves and SmartSite Y-sites and are labeled as DEHP FREE or with specific filter types.
Look for model numbers on the product packaging, such as 10013186, 2452-0007, or 2204-0007.
The infusion pump modules used with these sets may perform outside safe performance ranges for flow rate, bolus accuracy, and occlusion alarms.
Affected models include 10013186, 2452-0007, 2204-0007, and others listed with specific back check valves and SmartSite Y-sites.
No, but you should check your model number and contact CareFusion if you have one of the affected models.
We’ve drafted a message you can send BD Alaris to request your refund or repair — edit it as you like.
Subject: Recall Z-2180-2025 — BD Alaris BD Alaris Hello, I own a BD Alaris that is covered by recall Z-2180-2025 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.
