Social Engineering Drives 88% of Healthcare Cybersecurity Losses
A new report finds that average cyber insurance claim severity in the healthcare sector exceeded $2 million per incident in 2025.
Category: Standards
Standards
Latest
Standards
Latest
GE HealthCare’s Photonova Spectra Photon-counting CT Receives FDA Clearance
The cleared system introduces photon-counting CT designed to capture spectral data in a single scan and reduce protocol complexity.
Fresenius Kabi Issues Critical Software Update for Ivenix Infusion Pumps
FDA identifies Class I recall as most serious type due to software anomalies that may cause unexpected shutdowns and interface freezing.
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Why the Service Manual is the Master Key to the HTM Device Lifecycle
Service manuals aren’t optional or proprietary “extras” in a hospital. They’re required for safe maintenance and compliance, and they should be non-negotiable at purchase.
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New FDA-Approved Therapy Brings At-Home Electrical Field Treatment to Pancreatic Cancer Care
The wearable system uses alternating electrical fields to disrupt cancer cell division and can be used continuously during daily activities.
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GE HealthCare Receives FDA Clearance for Three New MRI Systems
The SIGNA portfolio includes a helium-free 1.5T system, advanced 3T scanner, and AI-driven workflow platform designed to improve imaging efficiency.
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FDA Clears Cardiovascular Monitoring Software for Surgical and ICU Settings
Argos Infinity analyzes existing physiologic data streams to provide early detection of hemodynamic instability without requiring new bedside hardware.
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FDA Clears Medtronic Robotic Spine Surgery System
The system brings surgical planning, real-time navigation, and robotic capabilities together in a single platform designed for spine procedures
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FDA Clears 3T Neonatal MRI System Designed for Use in the NICU
The system features a compact footprint and is designed for whole-body imaging in neonatal care settings.
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FDA Updates Medical Device Cybersecurity Guidance to Address New Federal Requirements
Revised guidance aligns with quality management system regulation changes and provides recommendations for cyber device submissions under section 524B of the FD&C Act.
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What 2025’s Healthcare Breaches Taught Us and Why 2026 Raises the Stakes
Lessons from 2025’s breaches point to a tougher reality in 2026, as AI adoption accelerates and cybersecurity becomes inseparable from patient care.
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FDA Clears Mobile C-Arm System With AI-Enhanced Imaging
The mobile C-arm system features AI-powered imaging tools and cable-free design for interventional procedures.
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AI Chatbots Top Annual List of Health Technology Hazards
ECRI’s report also sounds the alarm on insufficient planning for systems outages, substandard medical products, missed recalls of home diabetes management devices, and more.
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GAO Report Finds FDA Struggles to Meet Medical Device Recall Termination Goals
The agency exceeded its three-month termination timeline for 74% of recalls during fiscal years 2020-2024, due to staff constraints that limited oversight activities, the report finds.
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