The U.S. FDA is alerting healthcare providers to no longer implant end-stage heart failure patients with Medtronic’s Heartware Ventricular Assist Device System due to safety concerns.
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FDA deemed Boston Scientific’s recall of the Vici SDS and RDS venous stent system a Class I recall, reports MDDI.
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Nearly 90% of automated external defibrillators, or AEDs, are located outside the hospital. But who’s maintaining these life-saving devices? Here’s how you can help, according to Dr. Binseng Wang.
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The U.S. FDA has categorized a recall of Abbot pacemakers caused by a manufacturing process that allowed moisture into the devices as a Class I event; some devices containing the fault could still be in use, reports MedTech Dive.
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Pacific Medical Group is recalling the Alaris Infusion Pump Module Model 8100 because the front bezel components may crack or separate.
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