Baxter (NYSE:BAX) issued an urgent medical device correction notice regarding its Novum IQ syringe infusion pump.
A few weeks ago, the FDA deemed a Novum IQ recall Class I because the pump may incorrectly indicate the completion of an infusion.
Deerfield, Illinois-based Baxter notified customers of the latest issue in October. This correction comes as a result of the potential for an incomplete infusion following one or more downstream occlusion alarms. The company has work underway on a software upgrade and has not received reports of serious injury related to the issue.
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