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Early Alert: Infusion Pump Issue from Baxter
The FDA is aware that Baxter has issued a letter to affected customers recommending all Novum IQ Large Volume Pumps (LVP) and Novum IQ Syringe Pumps (SP) be corrected prior to use. These recommendations are based on software anomalies that may result in a blank Run screen for the LVP and SP, and/or false motor movement system error with the SP.
As of July 21, Baxter has received three reports of serious injuries and no reports of deaths related to these issues.
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program. The FDA has become aware of a potentially high-risk device issue. The FDA will keep the public informed and update this web page as significant new information becomes available.
Questions?
Customers in the U.S. with adverse reactions, quality problems, or questions about this recall should contact Baxter at corporate_product_complaints_round_lake@baxter.com or 1-800-843-7867 (select option 2, then option 2 again).
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