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Food and Drug Administration

Judge
National

U.S. District Court Issues Permanent Injunction Against Rizo Lopez Foods Following Listeria Outbreak

October 15, 2024October 14, 2024 - by Maryann Pugh

WASHINGTON, D.C. — The U.S. District Court for the Eastern District of California recently enforced a consent decree of permanent injunction against Rizo Lopez Foods Inc., a California-based food manufacturer, …

U.S. District Court Issues Permanent Injunction Against Rizo Lopez Foods Following Listeria Outbreak Read More

U.S. Food and Drug Administration (FDA)
Infectious Diseases / National

FDA Authorizes Groundbreaking Healgen Rapid Check COVID-19/Flu A&B Antigen Test

October 15, 2024October 14, 2024 - by Maryann Pugh

WASHINGTON, D.C. — The U.S. Food and Drug Administration (FDA) has granted marketing authorization for the Healgen Rapid Check COVID-19/Flu A&B Antigen Test. This innovative test marks a significant advancement …

FDA Authorizes Groundbreaking Healgen Rapid Check COVID-19/Flu A&B Antigen Test Read More
Korean Seasoned Seaweed
National

FDA Announcement: Recall of Shirakiku Korean Seasoned Seaweed Due to Undeclared Sesame Allergen

October 13, 2024October 12, 2024 - by Maryann Pugh

WASHINGTON, D.C. — The Food and Drug Administration (FDA) has issued a recall notice for 3.52-ounce packages of Shirakiku brand Korean Seasoned Seaweed, distributed by Wismettac Asian Foods, Inc. based …

FDA Announcement: Recall of Shirakiku Korean Seasoned Seaweed Due to Undeclared Sesame Allergen Read More

Enoki Mushroom 5.3 oz
National

FDA Issues Recall on Enoki Mushrooms Amid Listeria Concerns

October 12, 2024October 12, 2024 - by Maryann Pugh

WASHINGTON, D.C. — The Food and Drug Administration (FDA) has announced a voluntary recall by Enoki King Mushroom Farm, based in Ventura, California, involving its 5.3-ounce packages of Enoki Mushrooms. …

FDA Issues Recall on Enoki Mushrooms Amid Listeria Concerns Read More
Cachapa de Maiz sweet corn pancakes
National

Urgent Recall: Undeclared Wheat in Sweet Corn Pancakes Sparks Allergy Alert

October 12, 2024October 12, 2024 - by Maryann Pugh

WASHINGTON, D.C. — In a recent announcement, the Food and Drug Administration (FDA) has alerted consumers to a recall initiated by TIPICAL LATIN FOOD CORP based in Miami, Florida. The recall …

Urgent Recall: Undeclared Wheat in Sweet Corn Pancakes Sparks Allergy Alert Read More

Express Meal Kit
National

Reser’s Fine Foods Recalls Meal Kits Over Listeria Concerns

October 12, 2024October 12, 2024 - by Maryann Pugh

WASHINGTON, D.C. — In a recent announcement, the Food and Drug Administration (FDA) disclosed that Reser’s Fine Foods has initiated a voluntary recall of certain meal kits. This action stems …

Reser’s Fine Foods Recalls Meal Kits Over Listeria Concerns Read More
Assorted vegetables
National

FDA Launches Human Foods Program Amid Major Agency Reorganization

October 11, 2024October 10, 2024 - by Maryann Pugh

WASHINTON, D.C. — The U.S. Food and Drug Administration (FDA) recenlty announced the launch of its new Human Foods Program, marking the largest reorganization in the agency’s modern history. This …

FDA Launches Human Foods Program Amid Major Agency Reorganization Read More

Ocugen
Research

FDA Greenlights Ocugen’s Revolutionary Eye Treatment: What It Means for Vision Care

October 10, 2024October 9, 2024 - by Timothy Alexander

MALVERN, PA — Ocugen, Inc. (NASDAQ: OCGN) this week announced a pivotal development as the FDA lifted the clinical hold on its investigational drug application for OCU200.

FDA Greenlights Ocugen’s Revolutionary Eye Treatment: What It Means for Vision Care Read More
Product recall
National

FDA Announces Recall of Happy Moose Juice Products Over Safety Concerns

October 9, 2024October 8, 2024 - by Maryann Pugh

WASHINGTON, D.C. — The Food and Drug Administration has announced a voluntary recall by Youngstown Grape Distributors Inc., a co-manufacturer for Happy Moose Juice. The recall affects specific lots of …

FDA Announces Recall of Happy Moose Juice Products Over Safety Concerns Read More
Food and Drug Administration
National

FDA Alerts Public to Philips Respironics Ventilator Correction Over In-Line Nebulizer Concerns

October 9, 2024October 8, 2024 - by Maryann Pugh

WASHINGTON, D.C. — The United States Food and Drug Administration has issued a crucial announcement concerning a voluntary correction by Philips Respironics regarding their Trilogy Evo series ventilators. This correction addresses …

FDA Alerts Public to Philips Respironics Ventilator Correction Over In-Line Nebulizer Concerns Read More

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