Baxter Corporation is issuing an urgent medical device correction related to two different software issues that occur during use. The first issue observed is due to incorrect reported delivered volume while an infusion is running. The second issue observed is an unexpected screen transition during the 'air still detected' alarm workflow. Baxter Corporation is issuing a follow-up urgent medical device correction communication due to the Novum IQ Large Volume Infusion Pump (LVP) may not execute bolus initiations/ cancellations or titration adjustments as expected by the user. Recall start date: October 20, 2022
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