Baxter Healthcare Corporation Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009. for the controlled administration of fluids. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009. for the controlled administration of fluids.
Brand
Baxter Healthcare Corporation
Lot Codes / Batch Numbers
All Serial Numbers
Products Sold
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Baxter Healthcare Corporation is recalling Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009. for the controlled due to System errors were noted following changes the customers implemented to the configuration of their network and server systems. Gateway Server System p. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Baxter initiated the recall by letter on 06/04/2021. The letter described the problem and the hazard involved, and requested the consignee Baxter Technical Assistance in advance of making changes to your network or server infrastructure supporting the pumps or the Baxter Gateway, as indicated in Baxter's Gateway Server Installation Handoff document which customers receive upon installation. The firm is developing a software patch for all Spectrum IQ infusion pumps.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026