Joint Commission Partners With STS and ACC on Outcomes-Based Cardiac Certification
The new certification will use existing clinical registry data from STS and ACC to measure patient outcomes while reducing reporting burden for hospitals.
Category: Standards
Standards
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Standards
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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.
Draeger Pulls Certain ErgoStar Catheter Mounts After Reports of Hose Cracking
The company is asking facilities to stop using affected mounts and return unused stock; cracks can cause leakage that may restrict ventilation if uncompensated.
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ECRI Leaders Share System-Level Falls Prevention Insights at National Patient Safety Meeting
ECRI leaders discussed how technologies such as AI-based monitoring and safety systems can affect falls prevention and why system-level evaluation is critical to avoid unintended risk.
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FDA Flags Recall Involving IMRIS MRI Systems Linked to Siemens 3T Magnet Issue
The recall affects IMPRIS Neuro III-SV models that use Siemens 3T magnets, citing a risk of blocked helium venting during a magnet quench.
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FDA Issues Recall Early Alert for Olympus Single-Use Ligating Devices
Olympus has updated use instructions after reports that the ligation loop may not release as expected, potentially requiring emergency intervention.
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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.
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Coalition Urges HHS to Withdraw Proposed HIPAA Security Rule
More than 100 healthcare organizations are calling on HHS to withdraw the proposed HIPAA Security Rule update and pursue a collaborative approach to cybersecurity standards.
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FDA Clears for Augmented Reality Navigation Platform for Neurosurgery
The system is designed to give surgeons a clear, real-time view of critical anatomy and planned trajectories.Â
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FDA to Accept De-identified Data for Certain Medical Devices Submissions
New guidance permits the use of de-identified data without requiring individual patient information in marketing submissions.Â
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Survey Reveals Disconnect Between Hospital Cybersecurity Goals and IoMT Device Risk Management Practices
43% of hospital security leaders name IoMT visibility as their top cybersecurity challenge, while internal process issues create the biggest obstacle to effective risk management.
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Advocacy Group Renews Push for Medical Right to Repair
US PIRG is surveying HTM professionals to document how repair restrictions affect patient care, downtime, and costs.
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What HTM Needs to Know About The Joint Commission’s New Accreditation Model
As Accreditation 360 rolls out in January 2026, the Joint Commission explains what’s changing, what isn’t, and how HTM teams can prepare.
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GE HeathCare Recalls Carestation Anesthesia Systems Due to Shutdown Risk
GE HealthCare is updating use instructions after reports certain systems may not switch to battery mode during AC power loss, potentially disrupting ventilation and agent delivery.
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