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: