Becton Dickinson Says FDA Designates 2 Products as Class I Recall
July 18 2019 - 8:03AM
Dow Jones News
By Chris Wack
Becton, Dickinson and Co. (BDX) said Thursday that two voluntary
recalls related to certain Alaris Pump Modules Model 8100 and
certain model codes and lot numbers of the Alaris Pump Infusion
Sets used with the Alaris Pump Model 8100 were designated as a
Class I recall by the U.S. Food and Drug Administration
The medical technology company said it has already notified
customers affected by these recalls. Both products were formerly
marketed under the CareFusion brand, which Becton Dickinson
acquired in March 2015.
The company said that both recalls have been associated with
medical device reporting submissions, several of which are
associated with serious injuries.
Becton Dickinson said that the Alaris Pump Modules Model 8100
were manufactured between April 2011 and June 2017, and it is
contacting customers to schedule replacement of the bezel
assemblies.
Write to Chris Wack at chris.wack@wsj.com
(END) Dow Jones Newswires
July 18, 2019 07:48 ET (11:48 GMT)
Copyright (c) 2019 Dow Jones & Company, Inc.
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