Recall of BD Alaris Pump Module Model 8100 with Guardrails and Suite MX software versions due to potential flow rate and bolus accuracy issues. Affected units have specific serial numbers.
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.
BD Alaris Pump Module Model 8100 with Guardrails and Suite MX software versions are being recalled because they may not deliver the correct flow rates or bolus doses. This could lead to incorrect medication delivery during infusion therapy.
The pump module may operate outside safe limits for flow rate and medication accuracy, which could cause incorrect dosing. This risk is particularly concerning during critical infusions like insulin delivery.
Patients using insulin or other medications via BD Alaris pumps with these specific model and software versions are affected. Those with the listed serial numbers are most at risk.
Check if your pump has the model number 8100 with Guardrails and Suite MX software. Affected units include specific serial numbers listed in the recall notice.
Identify if your pump is a BD Alaris Model 8100 with Guardrails and Suite MX software.
Reach out to CareFusion 303, Inc. for assistance with the recall process.
Affected serial numbers include 10885403222054, 10885403517723, 10885403810015, 10885403810039, and 10885403810046.
The recall does not require immediate discontinuation; however, you should check if your pump is affected and contact CareFusion for guidance.
The official recall notice does not specify a fix or remedy, so contact CareFusion 303, Inc. directly for assistance.
We’ve drafted a message you can send BD Alaris to request your refund or repair — edit it as you like.
Subject: Recall Z-2179-2025 — BD Alaris BD Alaris Hello, I own a BD Alaris that is covered by recall Z-2179-2025 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.
