Baxter recalls Novum IQ Syringe Pump (Product Code 40800BAXUS) due to false 'Infusion Complete' alarms after occlusions, risking incorrect medication delivery.
Baxter is issuing an Urgent Medical Device Correction for the Novum IQ Syringe Pump. Baxter identified that after multiple downstream occlusion alarms, the pump may display an Infusion Complete alarm even though uninfused fluid remains in the syringe.
Baxter is recalling its Novum IQ Syringe Pump because it may show a false 'Infusion Complete' alarm even when medication remains in the syringe. This could lead to incorrect dosing if the pump stops before the full dose is delivered.
The pump may display an 'Infusion Complete' alarm after multiple downstream occlusion alarms, even though uninfused fluid remains in the syringe. This could cause the pump to stop delivering medication before the full dose is administered, potentially leading to underdosing.
Healthcare professionals using the Novum IQ Syringe Pump for medication administration are most at risk. Patients receiving treatments via this pump could be affected if the false alarm leads to premature stopping of infusion.
The recalled product is the Novum IQ Syringe Pump with Product Code 40800BAXUS. All serial numbers are affected, but the specific model and code are listed in the recall notice.
Look for the product code 40800BAXUS on the pump's label to confirm if it is recalled.
The pump may show a false 'Infusion Complete' alarm after multiple occlusion alarms, which could lead to underdosing medication. However, the risk is low and the pump is still safe for use with proper monitoring.
Check the product code on your pump's label. The recalled model is Novum IQ Syringe Pump with Product Code 40800BAXUS, and all serial numbers are affected.
The recall does not require immediate action, but you should check the product code to confirm if it is affected. If it is, monitor the pump closely and contact Baxter for further guidance.
We’ve drafted a message you can send Baxter to request your refund or repair — edit it as you like.
Subject: Recall Z-0151-2024 — Baxter Baxter Hello, I own a Baxter that is covered by recall Z-0151-2024 from Baxter. 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.
