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Medtronic Recalls Evera, Viva, Brava, Claria, Amplia, Compia, and Visia Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy (CRT-Ds) Due to Risk of Shortened Battery Life

Medtronic’s Evera, Viva, Brava, Claria, Amplia, Compia, and Visia ICDs and CRT-Ds correct heart arrhythmia. Some devices may have shortened battery life.

http://www.fda.gov/medical-devices/medical-device-recalls/medtronic-recalls-evera-viva-brava-claria-amplia-compia-and-visia-implantable-cardioverter

 
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País suma 907 casos COVID-19 el miércoles, 877 el jueves y 914 hoy viernes: 222.544 casos COVID-19 totales

País suma 907 casos COVID-19 el miércoles, 877 el jueves y 914 hoy viernes: 222.544 casos COVID-19 totales

País suma 907 casos COVID-19 el miércoles, 877 el jueves y 914 hoy viernes: 222.544 casos COVID-19 totalesViernes 09 de abril, 2021. El país registró 907 casos nuevos de COVID-19 el miércoles 07 de abril, 877 el jueves 08 de abril y 914

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/746-noticias-2021/2085-pais-suma-907-casos-covid-19-el-miercoles-877-el-jueves-y-914-hoy-viernes-222-544-casos-covid-19-totales

 
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Medtronic Recalls Valiant Navion Thoracic Stent Graft System Due to Risk of Stent Fractures and Type III Endoleaks

The Medtronic Stent Graft System is used to repair descending thoracic aortic aneurysm. Use of the device may lead to stent fractures and endoleaks.

http://www.fda.gov/medical-devices/medical-device-recalls/medtronic-recalls-valiant-navion-thoracic-stent-graft-system-due-risk-stent-fractures-and-type-iii

 
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NS NY Distributor Inc Issues Voluntary Nationwide Recall of Premium OrgaZen 7000 and Ginseng Power 5000 Due to Presence of Undeclared Sildenafil and/or Tadalafil

NS NY Distributor Inc is voluntarily recalling all lots within expiry of Premium Orgazen 7000 and Ginseng Power 5000 capsules to the consumer level. FDA analyses has found the products to contain undeclared sildenafil and/or tadalafil. Sildenafil and tadalafil are known as phosphodiesterase (PDE-5)

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ns-ny-distributor-inc-issues-voluntary-nationwide-recall-premium-orgazen-7000-and-ginseng-power-5000

 
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Comisión Nacional de Vacunación y Epidemiología aprobó el uso de vacuna contra COVID-19 de AstraZeneca en Costa Rica

Comisión Nacional de Vacunación y Epidemiología aprobó el uso de vacuna contra COVID-19 de AstraZeneca en Costa Rica

Comisión Nacional de Vacunación y Epidemiología aprobó el uso de vacuna contra COVID-19 de AstraZeneca en Costa Rica 8 de abril del 2021. La Comisión Nacional de Vacunación y Epidemiología (CNVE) aprobó el uso de la vacuna contra COVID-19 de AstraZeneca.

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/746-noticias-2021/2084-comision-nacional-de-vacunacion-y-epidemiologia-aprobo-el-uso-de-vacuna-contra-covid-19-de-astrazeneca-en-costa-rica