Murilo Freitas – Página 83

SOBRE DETECCION DE PRESENCIA DE CRONOBACTER Y SALMONELLA EN FORMULAS INFANTILES EN POLVO DE MARCA: SIMILAC FORTIFICADOR DE LECHE MATERNA, ALIMENTUM O ELECARE DE ABBOTT NUTRICION.

19 de febrero 2022. El Ministerio de Salud, a través de la Dirección de Regulación de Productos de Interés Sanitario…

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/746-noticias-2021/2279-alerta-sanitaria-sobre-deteccion-de-presencia-de-cronobacter-y-salmonella-en-formulas-infantiles-en-polvo-de-marca-similac-fortificador-de-leche-materna-alimentum-o-elecare-de-abbott-nutricion

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ALERTA SANITARIA DETECCIÓN DE VENTA DEL PRODUCTO MOTHER`S MILK

Murilo Freitas - 17:31, 20 de febrero de 2022482

ALERTA SANITARIA

DETECCIÓN DE VENTA DEL PRODUCTO MOTHER`S MILK

18 de febrero 2022. El Ministerio de Salud, a través de la Dirección de Regulación de Productos de Interés Sanitario…

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/746-noticias-2021/2278-alerta-sanitaria-deteccion-de-venta-del-producto-mother-s-milk

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Family Dollar Stores Issues Voluntary Recall of Certain FDA-Regulated Products in Six States Including Drugs, Devices, Cosmetics, Foods

Murilo Freitas - 05:00, 17 de febrero de 2022326

Family Dollar,
Inc. is initiating a voluntary retail level product recall of certain products regulated by the U.S. Food and Drug Administration (FDA) that were stored and shipped to 404 stores from Family Dollar Distribution Center 202 in West Memphis, Arkansas from January 1, 2021 through the pre

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/family-dollar-stores-issues-voluntary-recall-certain-fda-regulated-products-six-states-including

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E25Bio Recalls COVID-19 Direct Antigen Rapid Tests That Are Not Authorized, Cleared, or Approved by the FDA and May Give False Results

Murilo Freitas - 05:00, 17 de febrero de 2022331

E25Bio COVID-19 Direct Antigen Rapid Tests are being recalled because they are not authorized, cleared, or approved for use by the FDA.

http://www.fda.gov/medical-devices/medical-device-recalls/e25bio-recalls-covid-19-direct-antigen-rapid-tests-are-not-authorized-cleared-or-approved-fda-and

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Baxter Issues Urgent Safety Communication to Reinforce Important Safety Information Regarding Upstream Occlusion Alarms for all Spectrum V8 and Spectrum IQ Infusion Pumps

Murilo Freitas - 05:00, 17 de febrero de 2022347

Baxter International Inc. announced today it has issued an Urgent Safety Communication to reinforce important safety information regarding upstream occlusion alarms for all Spectrum V8 and Spectrum IQ infusion pumps. Incorrect administration set setup and/or incomplete resolution of upstream occlusi

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/baxter-issues-urgent-safety-communication-reinforce-important-safety-information-regarding-upstream