Baxter Healthcare Corporation Dose IQ Safety Software used with Spectrum IQ Infusion Pump Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Dose IQ Safety Software used with Spectrum IQ Infusion Pump
Brand
Baxter Healthcare Corporation
Lot Codes / Batch Numbers
Software version: All libraries initially created with version 9.0.x
Products Sold
Software version: All libraries initially created with version 9.0.x
Baxter Healthcare Corporation is recalling Dose IQ Safety Software used with Spectrum IQ Infusion Pump due to Software issue: The defect creates a mismatch between linked drug identifiers (IDs) in the Dose IQ user interface (UI) and the binary drug library (B. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software issue: The defect creates a mismatch between linked drug identifiers (IDs) in the Dose IQ user interface (UI) and the binary drug library (BDL) loaded onto the Spectrum IQ pump.
Recommended Action
Per FDA guidance
The firm issued an Urgent Medical Device Correction notice by letter on July 7, 2021. The letter explained the issue and provided a temporary workaround which can be implemented until the new software tool is ready for distribution.
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