Categories rss Disposable Surgical Stapler Cartridge Correction: Ethicon Endo-Surgery, LLC Issues Correction for Endopath Echelon to Address Inadvertent Lockout During Surgical ProceduresMurilo Freitas - 04:00, 24 de July de 2025337 0 Ethicon Endo-Surgery is correcting the Endopath Echelon due to a potential surgical lockout that stops cutting or stapling and requires extra removal steps. http://www.fda.gov/medical-devices/medical-device-recalls/disposable-surgical-stapler-cartridge-correction-ethicon-endo-surgery-llc-issues-correction-endopath
Categories rss Arterial Cannula Recall: Edwards Lifesciences Removes Arterial Cannula due to Risk of Wire ExposureMurilo Freitas - 04:00, 23 de July de 2025361 0 Edwards recalls arterial cannulae due to risk of wire exposure that may cause serious patient harm. http://www.fda.gov/medical-devices/medical-device-recalls/arterial-cannula-recall-edwards-lifesciences-removes-arterial-cannula-due-risk-wire-exposure
Categories rss HHS, FDA and USDA Address the Health Risks of Ultra-Processed FoodsMurilo Freitas - 21:44, 22 de July de 2025357 0 HHS, FDA and USDA Address the Health Risks of Ultra-Processed Foodshttp://www.fda.gov/news-events/press-announcements/hhs-fda-and-usda-address-health-risks-ultra-processed-foods
Categories rss Mobile Lift Component Recall: Baxter Healthcare Corporation Removes Mobile Lift Component due to Risk of Improper AttachmentMurilo Freitas - 04:00, 22 de July de 2025407 0 Baxter is removing mobile lift components due to risk of false attachment, which may result in patient injury due to falls. http://www.fda.gov/medical-devices/medical-device-recalls/mobile-lift-component-recall-baxter-healthcare-corporation-removes-mobile-lift-component-due-risk
Categories RSS OPAS PAHO Director and CARICOM Secretary-General sign 2025-2029 Joint Subregional cooperation strategy to advance health and equity in the Caribbeanadmin - 20:06, 21 de July de 2025282 0 PAHO Director and CARICOM Secretary-General sign 2025-2029 Joint Subregional cooperation strategy to advance health and equity in the Caribbean Cristina Mitchell 22 Jul 2025
Categories rss HHS, FDA Praise Consumer Brands Association’s Vow to Remove Artificial Colors from America’s Food SupplyMurilo Freitas - 18:17, 21 de July de 2025294 0 HHS, FDA Praise Consumer Brands Association’s Vow to Remove Artificial Colors from America’s Food Supplyhttp://www.fda.gov/news-events/press-announcements/hhs-fda-praise-consumer-brands-associations-vow-remove-artificial-colors-americas-food-supply
Categories rss Manual Resuscitator Recall: SunMed Holdings, LLC Removes Adult Manual Resuscitator Devices Due to Incorrect Assembly of B/V FilterMurilo Freitas - 04:00, 21 de July de 2025280 0 Manual resuscitator recalled due to incorrect B/V filter assembly that could delay therapy. May cause hypoxia, hypercapnia, or death if used. http://www.fda.gov/medical-devices/medical-device-recalls/manual-resuscitator-recall-sunmed-holdings-llc-removes-adult-manual-resuscitator-devices-due
Categories rss Medical Procedure Kits Correction: Medline Industries, LP Issues Correction for Medline Craniotomy Kits Containing Codman Disposable Perforators Due to Risk for Device DisassemblyMurilo Freitas - 04:00, 21 de July de 2025208 0 Medline Craniotomy Kits are procedure convenience kits. Kits containing the Codman Disposable Perforator are being corrected by Medline Industries. http://www.fda.gov/medical-devices/medical-device-recalls/medical-procedure-kits-correction-medline-industries-lp-issues-correction-medline-craniotomy-kits
Categories rss Stanford faculty member George Tidmarsh, M.D., Ph.D. named Director of Center for Drug Evaluation and ResearchMurilo Freitas - 10:57, 20 de July de 2025249 0 Stanford faculty member George Tidmarsh, M.D., Ph.D. named Director of Center for Drug Evaluation and Researchhttp://www.fda.gov/news-events/press-announcements/stanford-faculty-member-george-tidmarsh-md-phd-named-director-center-drug-evaluation-and-research
Categories rss Continuous Ventilator (Respirator) Correction: Maquet Critical Care AB Updates Use Instructions for Servo Ventilator Systems Due to Risk of Inaccurate Compliance Measurement Leading to Improper Tidal Volume Delivery in Neonatal PatientsMurilo Freitas - 04:00, 20 de July de 2025380 0 Maquet is updating Servo Ventilator instructions due to a risk of inaccurate tidal volume delivery when the extended leak test is used. http://www.fda.gov/medical-devices/medical-device-recalls/continuous-ventilator-respirator-correction-maquet-critical-care-ab-updates-use-instructions-servo
