BD Advises Biomed Inspection of Dropped Alaris Pump Modules
The company advises taking any dropped or severely jarred modules out of service and sending them to biomedical engineering for inspection before reuse.
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AAMI Foundation Awards $45,000 in Grants to Sterilization Projects
The AAMI Foundation has awarded more than $45,000 in Kilmer Fund Committee grants for projects on improving sterilization.
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BD Voluntarily Recalls Intraosseous Products
BD announced a voluntary recall on its Intraosseous Needle Set Kits, Intraosseous Manual Driver Kits, and Intraosseous Powered Drivers.
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BD Advises Biomed Inspection of Dropped Alaris Pump Modules
The company advises taking any dropped or severely jarred modules out of service and sending them to biomedical engineering for inspection before reuse.
BD Releases Its Inaugural Cybersecurity Annual Report
Through the BD 2020 Cybersecurity Report, the company seeks to address cybersecurity challenges specific to healthcare and offer guidance about cybersecurity practices for working with medical device manufacturers.
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BD Notifies Users of BD Alaris Network Session Vulnerability
BD has issued a statement to make users aware of a BD Alaris 8015 PC Unit and BD Alaris Systems Manager Network Session Vulnerability.
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CME America Recalls BodyGuard Infusion System Administration Sets
BD subsidiary CME America announces a voluntary recall for all CME America BodyGuard Infusion System Administration Sets—used with the company’s BodyGuard infusion pumps—that were distributed beginning May 2016.
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