The new integration of Asimily with CCM provides a single platform for viewing all internet-connected assets to determine which assets or manufacturers are at risk of cybersecurity issues.
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The FDA received an additional 6,000 medical device reports January 1, 2023-March 31, 2023, related to PE-PUR foam used in Philips ventilators and other devices recalled in June 2021.
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These infusion system replacement batteries were recalled because a defect has diminished how long they can be used to run the system, which may cause the system to shut down an ongoing infusion.
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ECRI has announced the winners of its 2023 Alerts Impact Award, recognizing members of its Alerts Workflow solution for their outstanding implementation of recall management programs in healthcare organizations.
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RRD’s solution aims to ensure end-to-end support throughout the complex recall notification process for medical device companies.
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