Baxter Healthcare Recalls Dose IQ Software Version 9.0.x, Used with Spectrum IQ Infusion Pumps, for Software Defect That May Improperly Configure Drug and Fluid Delivery

Date: 08/12/2021

Product type: Medical Device

Recalled Product

• Dose IQ Safety Software (used with Spectrum IQ Infusion System)
• Product Code: 35723V091
• Software Version: All drug libraries initially created with version 9.0.x
• Distribution Dates: February 1, 2018 to January 1, 2019
• Devices Recalled in the U.S.: 61
• Date Initiated by Firm: July 7, 2021

US-FDA Link: https://www.fda.gov/medical-devices/medical-device-recalls/baxter-healthcare-recalls-dose-iq-software-version-90x-used-spectrum-iq-infusion-pumps-software