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CorgioMed LLC Issues Voluntary Nationwide Recall of All Lots of Leafree Instant Hand Sanitizer Aloe Vera Labeled as EDIBLE ALCOHOL

CorgioMed, LLC is voluntarily recalling all lots of Leafree Instant Hand Sanitizer-Aloe Vera, within expiry to the consumer level. The products are being recalled because they are labeled as “EDIBLE ALCOHOL”. Leafree Hand Sanitizer is an alcohol-based hand rub to be applied externally to reduce bac

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/corgiomed-llc-issues-voluntary-nationwide-recall-all-lots-leafree-instant-hand-sanitizer-aloe-vera

 
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Ministerio de Salud reitera cuidados en sitios de confluencia de personas

Ministerio de Salud reitera cuidados en sitios de confluencia de personas

Ministerio de Salud reitera cuidados en sitios de confluencia de personasMiércoles 02 de setiembre, 2020. El Ministro de Salud, Daniel Salas enfatizó hoy en los cuidados que se deben tener al realizar ciertas actividades...

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/741-noticias-2020/1872-ministerio-de-salud-reitera-cuidados-en-sitios-de-confluencia-de-personas

 
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Ministerio de Salud autoriza la reconversión de bares, cantinas y tabernas a restaurantes, sodas y cafeterías

Ministerio de Salud autoriza la reconversión de bares, cantinas y tabernas a restaurantes, sodas y cafeterías

Ministerio de Salud autoriza la reconversión de bares, cantinas y tabernas a restaurantes, sodas y cafeteríasMartes 01 de setiembre, 2020. El Ministerio de Salud dio a conocer hoy las disposiciones administrativas relativas a la reconversión de los establecimientos comerciales destinados a...

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/741-noticias-2020/1870-ministerio-de-salud-autoriza-la-reconversion-de-bares-cantinas-y-tabernas-a-restaurantes-sodas-y-cafeterias

 
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BD Provides Update on Previously Disclosed Recall of BD Alaris System Hardware

BD (Becton, Dickinson and Company) (NYSE: BDX), a leading global medical technology company, today provided an update on a previously announced voluntary recall of the BD Alaris™ System. Three of the situations described in this recall, which BD announced on June 30, 2020, have been designated as Cl

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bd-provides-update-previously-disclosed-recall-bd-alaris-system-hardware

 
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The Protein Shoppe, LLC Issues Voluntary Nationwide Recall of the “Red- E” Male Enhancement Tablet Due to the Presence of Undeclared Sildenafil

The Protein Shoppe, LLC is voluntarily recalling all lots of “Red-E” (Male Enhancement tablet) to the consumer level. This recall has been initiated after an FDA laboratory analysis found the product to contain undeclared sildenafil, a Phosphodiesterase-5 (PDE-5) inhibitor which is the active ingred

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/protein-shoppe-llc-issues-voluntary-nationwide-recall-red-e-male-enhancement-tablet-due-presence