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Marshals Seize Misbranded Drug Products at Maine Facility per FDA’s Request

  • FDA

On June 6, 2012, the U.S. Food and Drug Administration (“FDA”) announced the seizure of various drug products from a…

FDA Releases Draft Guidance Updating Warnings for Labeling of Albumin, Highlighting Risk of Creutzfeldt Jakob Disease

  • FDA

On June 11, 2012, the U.S. Food and Drug Administration (“FDA”) published a draft guidance document, entitled Draft Guidance for…

Study Prompts OIG to Call for Further Training of FDA Medical Device Reviewers

  • FDA

On June 5, 2012, the Office of the Inspector General (“OIG”) published a report entitled, “Executive Summary: Scientific Disagreements Regarding…

FDA Alerts Consumers of an Array of Dangers Associated with Reumofan Plus Supplement

  • FDA

On June 1, 2012, the U.S. Food and Drug Administration (“FDA”) issued an alert to consumers on the product Reumofan…

U.S. Marshals Seize Products from California Firm upon FDA ’s Repeated Finding of Violations

  • FDA

On May 22, 2012, the U.S. Food and Drug Administration (“FDA”) announced that U.S. Marshals, acting at the requests of…

FTC May Have Won Battle with POM Wonderful but Industry Appears to Have Won the War

  • FTC

On May 21, 2012, the Federal Trade Commission (“FTC”) announced that it has prevailed in its claim against POM Wonderful…

FDA Notifies Consumers of Supplement Recall after Discovery of Undeclared Drug Ingredients

  • FDA

On May 18, 2012, the U.S. Food and Drug Administration (“FDA”) published a press release announcing the voluntary recall of…

FDA Expands Use of Device to Detect both Viral and Bacterial Causes of Respiratory Infection

  • FDA

On May 15, 2012, the U.S. Food and Drug Administration (“FDA”) announced the clearance of expanded uses for the FilmArray…

FDA and FAAN Aim to Educate Public during Food Allergy Awareness Week

  • FDA

This week (May 13 – May 19, 2012) is recognized as Food Allergy Awareness Week (“FAAW”). FAAW was created by…

FDA Warns of Recall Due to Undeclared Milk Derivatives in Several Beverage Products

  • FDA

On May 10, 2012, the U.S. Food and Drug Administration (“FDA”) posted a press release on its website notifying consumers…