Navigating AI Liability in Healthcare Technology Management
As AI becomes embedded in medical equipment, HTM professionals must navigate new questions of accuracy, accountability, and risk.
As AI becomes embedded in medical equipment, HTM professionals must navigate new questions of accuracy, accountability, and risk.
The voluntary recall involves pump modules that may have been repaired with FR-110 bezels, which the company says can weaken over time and compromise safe infusion delivery.
The new location aims to shorten delivery times and support hospitals across Oklahoma and neighboring states with on-demand medical equipment.
As AI becomes embedded in medical equipment, HTM professionals must navigate new questions of accuracy, accountability, and risk.
The FDA has issued an early alert regarding Baxter’s recall of certain Spectrum infusion pumps due to missing motor mounting screws, which may have occurred during servicing.
Read MoreAccurate Biomed will support CAIRE customers with in-warranty repairs, including the FreeStyle Comfort portable oxygen concentrator and the company’s line of stationary oxygen concentrator products.
Read MoreBaxter is recalling certain Solution Sets with Duo-Vent Spikes due to an assembly issue that led to inverted slide clamps.
Read MoreFresenius Kabi recalled a specific lot of Ivenix LVP Primary Administration Sets due to a defect that could cause uncontrolled flow.
Read MoreInspira Technologies introduced the INSPIRA Cardi-ART, a portable modular device that provides oxygen to the brain during cardiac arrest.
Read MoreOptumHealth Care Solutions is recalling Nimbus II Plus infusion pumps due to multiple failure modes, following an InfuTronix recall.
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The FDA has issued a warning to Cardinal Health for marketing unapproved Monoject syringes, highlighting safety risks and compliance issues.