In a warning letter, the Food and Drug Administration said Glenmark Pharmaceuticals failed to properly investigate flaws with ...

With hundreds of drug shortages persisting across the U.S., pharmacy leaders are adopting more coordinated strategies to manage supply disruptions and mitigate financial losses. These include ...

More than 67,000 cases of Power Stick roll-on deodorant products have been recalled. They were sold at Target, Walmart, ...

Reflow Medical, Inc., un leader dans le développement de dispositifs médicaux innovants pour le traitement des maladies cardiovasculaires complexes, a annoncé que la Food and Drug Administration (FDA) ...

La FDA accorde l'autorisation De Novo au Spur® Peripheral Retrievable Stent System de Reflow Medical ...

Deadly Defect In Infant Breathing Systems Prompts Urgent Recall, FDA Says A major infant ventilator component has been recalled because it could come apart during use, potentially causing organ ...

A digoxin-induced AV block usually improved (28 of 39) after withdrawal of the drug. Roughly half of the patients with drug-induced AV block underwent permanent PM implantation.

"The Zebra Neurovascular Access System was engineered to easily track through the tight bends of this delicate anatomy while maintaining lumen integrity, allowing for atraumatic deliverability in ...

Boston Scientific announced the FDA approval of expanded labeling for its pulsed field ablation system which now includes treatment of drug refractory, symptomatic persistent atrial fibrillation ...