rss-es – Página 83

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 2022281

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

rss-es

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 2022290

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

rss rss-es rss-pt

BASE10 Genetics Recalls RNAstill MTM Specimen Collection Kits That Are Not Authorized, Cleared, or Approved by the FDA, May Give False Results, and Require Special Training for Safe Handling

Murilo Freitas - 05:00, 17 de febrero de 2022317

BASE10 Genetics RNAstill MTM specimen collection kits are being recalled because they are not FDA-authorized, -cleared, or -approved for use.

http://www.fda.gov/medical-devices/medical-device-recalls/base10-genetics-recalls-rnastill-mtm-specimen-collection-kits-are-not-authorized-cleared-or-approved

rss-es

Do Not Use E25Bio COVID-19 Tests: FDA Safety Communication

Murilo Freitas - 05:00, 17 de febrero de 2022312

The FDA is warning people not to use the E25Bio COVID-19 Direct Antigen Rapid Test. The FDA is concerned about the risk of false results when using this test.

http://www.fda.gov/medical-devices/safety-communications/do-not-use-e25bio-covid-19-tests-fda-safety-communication

rss-es

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 2022262

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

rss-es

Salud decomisa 2.924 unidades de productos ilegales

Murilo Freitas - 19:38, 16 de febrero de 2022358

Salud decomisa 2.924 unidades de productos ilegales

Jueves 17 de febrero, 2022. El Ministerio de Salud en conjunto con la Policía de Control Fiscal…

https://www.ministeriodesalud.go.cr/index.php/centro-de-prensa/noticias/746-noticias-2021/2277-salud-decomisa-2-924-unidades-de-productos-ilegales

rss rss-es rss-pt

Vyaire Medical Recalls bellavista 1000 and 1000e Series Ventilators Due to Issues with Software Configurations

Murilo Freitas - 05:00, 16 de febrero de 2022317

There is an issue with bellavista 1000 and 1000e ventilators with software version 6.0.1600.0 or higher installed and have the Data Communication port set to “HL7.»

http://www.fda.gov/medical-devices/medical-device-recalls/vyaire-medical-recalls-bellavista-1000-and-1000e-series-ventilators-due-issues-software

rss-es

TCP HOT Acquisition LLC dba HRB Brands Issues Voluntary Nationwide Recall of Sure and Brut Aerosol Sprays Due to the Presence of Benzene

Murilo Freitas - 05:00, 15 de febrero de 2022417

Westport, Connecticut, TCP HOT Acquisition LLC dba HRB Brands is voluntarily recalling all lot numbers with expiration dates on or before August 2023 of the Sure and Brut Aerosol Sprays listed in the table below to the consumer level due to the presence of benzene. While benzene is not an ingredient

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/tcp-hot-acquisition-llc-dba-hrb-brands-issues-voluntary-nationwide-recall-sure-and-brut-aerosol

rss-es