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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 2022290

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 2022298

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

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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 2022325

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

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

Murilo Freitas - 05:00, 17 de febrero de 2022320

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

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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 2022271

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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Salud decomisa 2.924 unidades de productos ilegales

Murilo Freitas - 19:38, 16 de febrero de 2022382

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

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

Murilo Freitas - 05:00, 16 de febrero de 2022325

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

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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 2022429

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

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