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Countries of the Americas advance toward regional strategy to tackle the health threat from venomous animal accidents

admin - 14:10, 21 de August de 2025303

Countries of the Americas advance toward regional strategy to tackle the health threat from venomous animal accidents

Cristina Mitchell

22 Aug 2025

Vascular Stent Recall: Boston Scientific Removes Carotid WALLSTENT Monorail Endoprosthesis Due to Risk of Resistance During Device Withdrawal

Murilo Freitas - 04:00, 21 de August de 2025334

Boston Scientific Removes Carotid WALLSTENT Monorail Endoprosthesis due to risk of resistance during device withdrawal

http://www.fda.gov/medical-devices/medical-device-recalls/vascular-stent-recall-boston-scientific-removes-carotid-wallstent-monorail-endoprosthesis-due-risk

HHS Allows FDA Emergency Use of Animal Drugs to Combat New World Screwworm, Protect U.S. Food Supply

Murilo Freitas - 12:45, 18 de August de 2025289

HHS Allows FDA Emergency Use of Animal Drugs to Combat New World Screwworm, Protect U.S. Food Supply
http://www.fda.gov/news-events/press-announcements/hhs-allows-fda-emergency-use-animal-drugs-combat-new-world-screwworm-protect-us-food-supply

B. Braun Medical Issues Voluntary Nationwide Recall of Lactated Ringer’s Injection USP 1000 mL and 0.9% Sodium Chloride Injection USP 1000 mL Due to the Presence of Particulate Matter

Murilo Freitas - 04:00, 18 de August de 2025400

For Immediate Release – BETHLEHEM, PA – August 19, 2025 – B. Braun Medical Inc. (B. Braun) is voluntarily recalling two lots of Lactated Ringers Injection USP 1000 mL,and 0.9% Sodium Chloride Injection USP 1000 mL to the hospital level due to the presence of particulate matter inside the container.

http://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/b-braun-medical-issues-voluntary-nationwide-recall-lactated-ringers-injection-usp-1000-ml-and-09

Ten countries in the Americas report measles outbreaks in 2025

admin - 13:04, 14 de August de 2025513

Ten countries in the Americas report measles outbreaks in 2025

Cristina Mitchell

15 Aug 2025

Early Alert: Cardiac Cannula Issue from Medtronic

Murilo Freitas - 04:00, 14 de August de 2025242

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program

http://www.fda.gov/medical-devices/medical-device-recalls/early-alert-cardiac-cannula-issue-medtronic

Early Alert: Infusion Pump Issue from Baxter

Murilo Freitas - 04:00, 14 de August de 2025226

Correction Issued for the Novum IQ Large Volume Pumps, Syringe Pumps

http://www.fda.gov/medical-devices/medical-device-recalls/early-alert-infusion-pump-issue-baxter-0

FDA Approves First Immunotherapy for Recurrent Respiratory Papillomatosis

Murilo Freitas - 22:11, 13 de August de 2025289

FDA Approves First Immunotherapy for Recurrent Respiratory Papillomatosis
http://www.fda.gov/news-events/press-announcements/fda-approves-first-immunotherapy-recurrent-respiratory-papillomatosis

PAHO publishes new update on Oropouche fever in the Americas

admin - 12:30, 13 de August de 2025326

PAHO publishes new update on Oropouche fever in the Americas

Cristina Mitchell

14 Aug 2025

Statement from FDA Commissioner Marty Makary, M.D., M.P.H., on Florida Restriction of 7-OH Opioid Products

Murilo Freitas - 18:43, 12 de August de 2025240

Statement from FDA Commissioner Marty Makary, M.D., M.P.H., on Florida Restriction of 7-OH Opioid Products
http://www.fda.gov/news-events/press-announcements/statement-fda-commissioner-marty-makary-md-mph-florida-restriction-7-oh-opioid-products

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