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Aumento exponencial de casos obliga a adelantar medidas de cierre: 649 nuevos positivos

Aumento exponencial de casos obliga a adelantar medidas de cierre: 649 nuevos positivos

Aumento exponencial de casos obliga a adelantar medidas de cierre: 649 nuevos positivosJueves 9 de julio, 2020. El país contabiliza hoy el mayor aumento de casos COVID-19, con 649 nuevos positivos

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/741-noticias-2020/1776-aumento-exponencial-de-casos-obliga-a-adelantar-medidas-de-cierre-649-nuevos-positivos

 
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MIVAH, Ministerio de Salud y CFIA realizan inspecciones en construcciones ubicadas en zonas anaranjadas

MIVAH, Ministerio de Salud y CFIA realizan inspecciones en construcciones ubicadas en zonas anaranjadas

 MIVAH, Ministerio de Salud y CFIA realizan inspecciones en construcciones ubicadas en zonas anaranjadasJueves 09 de julio 2020. Funcionarios del Ministerio de Vivienda y Asentamientos Humanos y del Ministerio de Salud, efectúan desde esta semana inspecciones a diferentes obras constructivas del país

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/741-noticias-2020/1775-mivah-ministerio-de-salud-y-cfia-realizan-inspecciones-en-construcciones-ubicadas-en-zonas-anaranjadas

 
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5836 casos confirmados por COVID-19

5836 casos confirmados por COVID-19

5836 casos confirmados por COVID-19Miércoles 8 de julio, 2020. Al 8 de julio se registran 350 nuevos casos de COVID-19, para un total de 5836 casos confirmados, con un rango de edad de cero a 96 años. Se trata de 2476 mujeres y 3360 hombres, de los cuales 4130 son costarricenses y 1706 son extranjeros.

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/741-noticias-2020/1770-5836-casos-confirmados-por-covid-19

 
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Endologix Issues Correction Notice for Ovation iX Abdominal Stent Graft System

Endologix® Inc. (Nasdaq: ELGX) (“Endologix” or the “Company”), a developer and marketer of innovative treatments for aortic disorders, today announced that a correction notice has been issued for the Ovation iX system, that identifies the root cause of polymer leaks. This voluntary action has been c

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/endologix-issues-correction-notice-ovation-ix-abdominal-stent-graft-system

 
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CME America Announces a Follow-Up on the Voluntary Recall of BodyGuard® Infusion System Administration Sets

As part of CME America’s commitment to quality, following the previously announced recall (April 27, 2020) of the BodyGuard® Infusion Pump Systems, the company conducted additional flow-rate accuracy testing. This testing revealed that some infusion sets do not meet the ±5% delivery accuracy for the

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/cme-america-announces-follow-voluntary-recall-bodyguardr-infusion-system-administration-sets

 
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Lupin Pharmaceuticals, Inc. Issues Voluntarily Nationwide Recall of Metformin Hydrochloride Extended-Release Tablets, 500mg and 1000mg Due to the Detection of N-Nitrosodimethylamine (NDMA) Impurity

Lupin Pharmaceuticals Inc. is voluntarily recalling all batches of Metformin Hydrochloride Extended-Release Tablets USP, 500mg and 1000mg to the consumer level. As part of the ongoing assessment and continuation of the dialog with the FDA, additional analysis revealed that certain tested batches wer

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lupin-pharmaceuticals-inc-issues-voluntarily-nationwide-recall-metformin-hydrochloride-extended