Washington, D.C.--(Newsfile Corp. - December 16, 2024) - The Securities and Exchange Commission today announced settled charges against Becton, Dickinson and Company, a New Jersey-based medical device ...

Co announces it has reached an agreement with the F.D.A on a consent decree regarding its Alaris SE line of infusion pumps. The agreement, which is subject to approval by the U.S. District Court for ...

This story was originally published on MedTech Dive. To receive daily news and insights, subscribe to our free daily MedTech Dive newsletter. BD has expanded a Class I Alaris recall to cover 15 ...

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The U.S. FDA said that BD (NYSE:BDX) has expanded its Class I voluntary recall to inform customers about the worst-case performance of the BD Alaris Pump Module model 8100 when used with certain ...

BD CEO Tom Polen noted that the newly FDA-cleared Alaris infusion pump system “addresses all open recalls,” spanning recent hardware, software and cybersecurity issues. (BD) Since the start of 2020, ...

The US Food and Drug Administration (FDA) has notified healthcare providers of a class 1 recall of CareFusion's Alaris PC unit (model 8015) with software version 9.12. The Alaris PC unit is the ...

The Syndeo pump could be reintroduced after Baxter fixes its design problems. CDRH has historically been suspicious about the reliability of infusion pumps. Incidents with two pump makers in 2006 have ...

Please provide your email address to receive an email when new articles are posted on . The FDA granted 510(k) clearance to Becton Dickinson’s updated Alaris infusion pump, allowing the company to ...

BD gave one of the identified issues a score of 8.2 on the 10-point Common Vulnerability Scoring System, denoting its high severity. The other seven cybersecurity risks, meanwhile, were given low- to ...

Security vulnerabilities have been found in a series of builds of Becton, Dickinson and Company Alaris Gateway Workstations, which are used to provide mounting, power and communication support to ...