rss-es – Página 12 – PRAIS 2.0

Joint Federal Operation Results in Seizure of More Than $18 Million in Illegal E-Cigarettes

Murilo Freitas - 15:44, 13 de diciembre de 2023217

Joint Federal Operation Results in Seizure of More Than $18 Million in Illegal E-Cigarettes
http://www.fda.gov/news-events/press-announcements/joint-federal-operation-results-seizure-more-18-million-illegal-e-cigarettes

FDA Warns Nine Manufacturers, Distributors of Unapproved Antimicrobials for Animals

Murilo Freitas - 13:59, 13 de diciembre de 2023195

FDA Warns Nine Manufacturers, Distributors of Unapproved Antimicrobials for Animals
http://www.fda.gov/news-events/press-announcements/fda-warns-nine-manufacturers-distributors-unapproved-antimicrobials-animals

FDA Advances Reorganization Proposal for Unified Human Foods Program, Field Operations and Additional Modernization Efforts

Murilo Freitas - 17:58, 12 de diciembre de 2023225

FDA Advances Reorganization Proposal for Unified Human Foods Program, Field Operations and Additional Modernization Efforts
http://www.fda.gov/news-events/press-announcements/fda-advances-reorganization-proposal-unified-human-foods-program-field-operations-and-additional

FDA Creates New Advisory Committee for Evaluation of Genetic Metabolic Disease Treatments

Murilo Freitas - 14:49, 11 de diciembre de 2023315

FDA Creates New Advisory Committee for Evaluation of Genetic Metabolic Disease Treatments
http://www.fda.gov/news-events/press-announcements/fda-creates-new-advisory-committee-evaluation-genetic-metabolic-disease-treatments

FDA Roundup: December 8, 2023

Murilo Freitas - 19:10, 7 de diciembre de 2023217

FDA Roundup: December 8, 2023
http://www.fda.gov/news-events/press-announcements/fda-roundup-december-8-2023

FDA Approves First Gene Therapies to Treat Patients with Sickle Cell Disease

Murilo Freitas - 16:10, 7 de diciembre de 2023308

FDA Approves First Gene Therapies to Treat Patients with Sickle Cell Disease
http://www.fda.gov/news-events/press-announcements/fda-approves-first-gene-therapies-treat-patients-sickle-cell-disease

Getinge Recalls CARDIOHELP Emergency Drive due to an Impaired or Inability to Turn the Drive

Murilo Freitas - 05:00, 7 de diciembre de 2023204

Getinge is recalling the CARDIOHELP Emergency Drive because it can become stuck or difficult to turn due to friction being generated in the handle attachment.

http://www.fda.gov/medical-devices/medical-device-recalls/getinge-recalls-cardiohelp-emergency-drive-due-impaired-or-inability-turn-drive

Carefully Monitor Philips DreamStation 2 CPAP Machines for Signs of Overheating: FDA Safety Communication

Murilo Freitas - 05:00, 6 de diciembre de 2023305

Reports of smoke, sparks, fire, and burns stemming from use of the DreamStation2 CPAP machines prompt warning from the FDA.

http://www.fda.gov/medical-devices/safety-communications/carefully-monitor-philips-dreamstation-2-cpap-machines-signs-overheating-fda-safety-communication

FDA Roundup: December 5, 2023

Murilo Freitas - 21:59, 4 de diciembre de 2023215

FDA Roundup: December 5, 2023
http://www.fda.gov/news-events/press-announcements/fda-roundup-december-5-2023

Cordis US Corp Recalls INFINITI Angiographic Catheter due to Products Being Shipped Without Undergoing Sterilization Procedures

Murilo Freitas - 05:00, 4 de diciembre de 2023211

The Cordis INFINITI Angiographic Catheter is being recalled due to some of the products being shipped to end users without undergoing sterilization procedures.

http://www.fda.gov/medical-devices/medical-device-recalls/cordis-us-corp-recalls-infiniti-angiographic-catheter-due-products-being-shipped-without-undergoing