Baxter International's Baxter Healthcare Corp. is recalling some of its infusion pumps over a serious system error, according to the FDA.The FDA on Thursday designated the recall as Class I.Regulators ...

The FDA is spotlighting a new medical device correction effort at Baxter over its large-volume Novum IQ infusion pump, following reports of 79 serious injuries and two deaths linked to potential under ...

Add Yahoo as a preferred source to see more of our stories on Google. Fresenius Kabi recalled some of its large volume infusion pumps over a software problem that can lead to delays or interruptions ...

The use of smart pump technology has been proven to reduce the frequency of errors in the administration of intravenous drugs. But software glitches and other potentially dangerous problems persist.

Baxter has issued a correction for its Novum IQ Large Volume Pumps and Novum IQ Syringe Pumps. All Novum large volume and syringe pumps have a software anomaly that ...

Of the roughly 1.5 million adverse drug events are reported annually to the FDA, more than half are attributed to infusion-related errors. The automated pumps that ...

Drug delivery devices are in the safety regulation crosshairs as of late, as a growing list of the technologies have found themselves the subject of recalls and corrections in recent weeks. Latest to ...