Baxter recalls Spectrum IQ Infusion System with Dose IQ Safety Software (Product Code 3570009) due to network configuration errors causing pump connectivity issues. Affected units may experience infusion errors.
System errors were noted following changes the customers implemented to the configuration of their network and server systems. Gateway Server System performance anomalies resulted in excessive Spectrum IQ pump connectivity errors.
Baxter is recalling its Spectrum IQ Infusion System with Dose IQ Safety Software (Product Code 3570009) because network configuration changes can cause the pump to disconnect from the system. This could lead to infusion errors if the pump loses connection during treatment.
Network configuration errors can cause the pump to disconnect from the system. This may lead to infusion errors if the pump loses connection during treatment. The issue occurs when customers change their network or server settings after the system was installed.
Patients using the Spectrum IQ Infusion System with Dose IQ Safety Software (Product Code 3570009) for fluid administration are affected. Healthcare providers who have made network configuration changes to this system are most at risk.
Check for the product code 3570009 on the device. The system is used for controlled fluid administration and has all serial numbers listed.
Review network and server settings to ensure they haven't been changed after installation.
Baxter recalls this system because network configuration changes can cause pump connectivity errors, potentially leading to infusion errors.
The recall does not specify a return or replacement process. Check your network configuration to prevent disconnections.
The recall notes potential infusion errors but does not mention serious injury risks. The hazard level is low risk.
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-2110-2021 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-2110-2021 from Baxter Healthcare. 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.
