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.
The company advises taking any dropped or severely jarred modules out of service and sending them to biomedical engineering for inspection before reuse.
The AAMI Foundation has awarded more than $45,000 in Kilmer Fund Committee grants for projects on improving sterilization.
BD announced a voluntary recall on its Intraosseous Needle Set Kits, Intraosseous Manual Driver Kits, and Intraosseous Powered Drivers.
The company advises taking any dropped or severely jarred modules out of service and sending them to biomedical engineering for inspection before reuse.
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.
Read MoreBD has issued a statement to make users aware of a BD Alaris 8015 PC Unit and BD Alaris Systems Manager Network Session Vulnerability.
Read MoreBD 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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