Becton Dickinson (NYSE:BDX) said today it has updated two voluntary recalls of certain Alaris infusion pump modules and infusion sets used with those modules.
The FDA has designated both recalls as Class I, as the agency has received reports of several serious injuries associated with the recalled devices.
The Alaris model 8100 modules were manufactured between April 2011 and June 2017. Both products were formerly marketed under the CareFusion brand, which BD acquired in March 2015.
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