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2020 aumentó en 8% la generación de residuos, en comparación al 2019

Murilo Freitas - 21:13, 3 de febrero de 2022328

2020 aumentó en 8% la generación de residuos, en comparación al 2019

2020 aumentó en 8% la generación de residuos, en comparación al 2019Viernes 04 de febrero, 2022. Durante el primero año de la pandemia (2020) los costarricenses produjeron un total de 1.459.288…

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/746-noticias-2021/2268-2020-aumento-en-8-la-generacion-de-residuos-en-comparacion-al-2019

 
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Vyaire Medical Issues Voluntary Correction for Certain bellavista™ Ventilators in Specific Software Configurations

Murilo Freitas - 05:00, 3 de febrero de 2022427
In December 2021, imtmedical ag, a subsidiary of Vyaire Medical, initiated a voluntary field correction for certain bellavista™ ventilators. With specific software version and configuration combinations, the ventilators can cease ventilation and generate a technical failure alarm 305. There is a pot

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vyaire-medical-issues-voluntary-correction-certain-bellavistatm-ventilators-specific-software

 
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Junp LLC Issues Voluntary Nationwide Recall of MegMan Performance Booster Capsules Due to the Presence of Tadalafil

Murilo Freitas - 05:00, 3 de febrero de 2022255
Brooklyn, NY Junp LLC is voluntarily recalling Lot number 2010291, Exp Date: 01/07/2024 of MegMan Performance Booster capsules, packaged in 10-count blisters packaged in a carton to the consumer level. Junp LLC was notified by Amazon that laboratory analysis has found the product to be tainted wit

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/junp-llc-issues-voluntary-nationwide-recall-megman-performance-booster-capsules-due-presence

 
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SD BIOSENSOR, Issues Notification of Voluntary Recall of ‘STANDARD Q COVID-19 Ag Home Test’

Murilo Freitas - 05:00, 3 de febrero de 2022370
Biosensor, Inc., a global in-vitro diagnostics company, is voluntarily recalling its STANDARD Q COVID-19 Ag Home Test in the United States, due to confirmed reports that the test kits were illegally imported into the United States. The STANDARD Q COVID-19 Ag Home Test is not authorized, cleared or a

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/sd-biosensor-issues-notification-voluntary-recall-standard-q-covid-19-ag-home-test

 
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Tercera dosis de vacuna contra COVID-19 puede aplicarse a cinco meses de haber completado esquema

Murilo Freitas - 21:48, 2 de febrero de 2022381

Tercera dosis de vacuna contra COVID-19 puede aplicarse a cinco meses de haber completado esquema

Tercera dosis de vacuna contra COVID-19 puede aplicarse a cinco meses de haber completado esquema3 de febrero de 2020. La Comisión Nacional de Vacunación y Epidemiología (CNVE) aprobó que a partir de hoy se reduzca a cinco…

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/746-noticias-2021/2267-tercera-dosis-de-vacuna-contra-covid-19-puede-aplicarse-a-cinco-meses-de-haber-completado-esquema

 
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Ukoniq (umbralisib): Drug Safety Communication – FDA Investigating Possible Increased Risk of Death with Lymphoma

Murilo Freitas - 05:00, 2 de febrero de 20221,934
The FDA is investigating a possible increased risk of death with the cancer medicine Ukoniq (umbralisib) approved to treat two specific types of lymphomas, which are cancers that affect the body’s immune system.

http://www.fda.gov/safety/medical-product-safety-information/ukoniq-umbralisib-drug-safety-communication-fda-investigating-possible-increased-risk-death-lymphoma

 
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Casos, hospitalizaciones y fallecimientos COVID-19 continúan registrando alzas

Murilo Freitas - 19:32, 31 de enero de 2022438

Casos, hospitalizaciones y fallecimientos COVID-19 continúan registrando alzas

Casos, hospitalizaciones y fallecimientos COVID-19 continúan registrando alzasMartes 1 de febrero, 2022. La semana epidemiológica 4 que abarcó del 23 al 29 de enero registró 39.611 casos de COVID-19…

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/746-noticias-2021/2266-casos-hospitalizaciones-y-fallecimientos-covid-19-continuan-registrando-alzas

 
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Esupplementsales, LLC Issues a Nationwide Recall All Lots of Hard Dawn Due to the Presence of Undeclared Tadalafil

Murilo Freitas - 05:00, 30 de enero de 2022352
Orangevale, CA, Esupplementsales, LLC is voluntarily recalling lot number 2107 of Hard Dawn Rise and Shine capsules to the consumer level. Esupplementsales, LLC was informed by Amazon that laboratory analysis has found the product to be tainted with tadalafil, an ingredient known as a phosphodieste

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/esupplementsales-llc-issues-nationwide-recall-all-lots-hard-dawn-due-presence-undeclared-tadalafil

 
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