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Espacio de diálogo promueve soluciones para mejorar la gestión de los residuos eléctricos y electrónicos

Espacio de diálogo promueve soluciones para mejorar la gestión de los residuos eléctricos y electrónicos

Espacio de diálogo promueve soluciones para mejorar la gestión de los residuos eléctricos y electrónicos13 de agosto del 2020. Más de 110 actores, entre municipalidades, instituciones, productores, importadores, unidades de cumplimiento ...

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/746-noticias-2021/2154-espacio-de-dialogo-promueve-soluciones-para-mejorar-la-gestion-de-los-residuos-electricos-y-electronicos

 
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Nuevo distanciamiento de un metro permitirá a más estudiantes asistir de forma presencial

Nuevo distanciamiento de un metro permitirá a más estudiantes asistir de forma presencial

Nuevo distanciamiento de un metro permitirá a más estudiantes asistir de forma presencial13 de Agosto, 2021. Una nueva distancia de un metro entre estudiantes, de la mano con un uso adecuado de la mascarilla dentro de las aulas...

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/746-noticias-2021/2153-nuevo-distanciamiento-de-un-metro-permitira-a-mas-estudiantes-asistir-de-forma-presencial

 
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Eight Medical International Recalls Recirculator 8.0 Disposable Lavage Kits due to Potential Exposure to High Levels of Aluminum

When used for warming therapy, the Recirculator 8.0 Disposable Lavage Kit from Eight Medical may expose patients to high levels of aluminum.

http://www.fda.gov/medical-devices/medical-device-recalls/eight-medical-international-recalls-recirculator-80-disposable-lavage-kits-due-potential-exposure

 
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Baxter Healthcare Recalls Dose IQ Software Version 9.0.x, Used with Spectrum IQ Infusion Pumps, for Software Defect That May Improperly Configure Drug and Fluid Delivery

A software defect in Baxter’s Dose IQ Software version 9.0.x may impact how fluid is delivered to a patient with the Spectrum IQ Infusion Pump

http://www.fda.gov/medical-devices/medical-device-recalls/baxter-healthcare-recalls-dose-iq-software-version-90x-used-spectrum-iq-infusion-pumps-software

 
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Medtronic Stops Distribution and Sale of HeartWare HVAD System Due to Risk of Neurological Adverse Events, Mortality, and Potential Failure to Restart

Increased risk of neurological adverse events, mortality and possible failure of the pump to restart led to stop sale and distribution of HeartWare HVAD System

http://www.fda.gov/medical-devices/medical-device-recalls/medtronic-stops-distribution-and-sale-heartware-hvad-system-due-risk-neurological-adverse-events

 
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Jongu 4308 Issues Voluntary Nationwide Recall of Hydro Pineapple Burn Due to the Presence of Undeclared Sibutramine.

[eBay Seller ID: jongu 4308] is voluntarily recalling all lots of Hydro Pineapple Burn to consumer level. FDA analysis has found the product to contain undeclared sibutramine. Sibutramine was an FDA approved drug used as an appetite suppressant for weight loss but was withdrawn from the market beca

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/jongu-4308-issues-voluntary-nationwide-recall-hydro-pineapple-burn-due-presence-undeclared