Baxter Novum IQ Syringe Pump, product code 40800BAXUS,
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Baxter has identified a design issue which may cause the pump to detect the presence of a syringe flange when no syringe is loaded. When this issue occurs, the pumps 'user interface becomes stuck on the "Remove Syringe" screen when an infusion is complete, and the syringe is unloaded. A System Error 21502 (Flange Sensor Failure) may occur. Please note this issue only affects a subset of Novum IQ syringe pumps manufactured or repaired after July 4, 2023.
What to do
FDA enforcement status: Ongoing
Brands named
UPCs
Recall history
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