Baxter Spectrum IQ Infusion System Recall: Network Errors Cause Pump Disconnects
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.
Lower-risk recall
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.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/62387-baxter-spectrum-iq-infusion-system-recall-network-errors-cause-pump.
Source Summary by GovInfoNow · govinfonow.com/recall/62387-baxter-spectrum-iq-infusion-system-recall-network-errors-cause-pump · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2110-2021
Cite this page
“Baxter Spectrum IQ Infusion System Recall: Network Errors Cause Pump Disconnects.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62387-baxter-spectrum-iq-infusion-system-recall-network-errors-cause-pump. Based on FDA recall #Z-2110-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2110-2021%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
Check for the product code 3570009 on the device. The system is used for controlled fluid administration and has all serial numbers listed.
- Brand
Baxter Healthcare- Category
Medical device
What to do — step by step
Check System Configuration
Review network and server settings to ensure they haven't been changed after installation.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “United States (including Puerto Rico), Canada, Bahamas, Bermuda, Guyana, and Trinidad and Tobago.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 3.3 years after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-2110-2021 (June 4, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2110-2021 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.