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Tag: FDA

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

Allergens, FDA, Food, Labeling, Recalls, Warning LettersFDA

This week (May 13 – May 19, 2012) is recognized as Food Allergy Awareness Week (“FAAW”). FAAW was created by the Food Allergy & Anaphylaxis Network (“FAAN”), a non-profit organization dedicated to promoting awareness food allergies and those who suffer …

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

Allergens, Beverages, FDA, Food, Labeling, Milk, RecallsFDA

On May 10, 2012, the U.S. Food and Drug Administration (“FDA”) posted a press release on its website notifying consumers of a recent recall of various fruit beverages. Jonlly Fruits Inc., the manufacturer of the beverages, opted to initiate the …

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FDA Announces Recall of Alfalfa Sprouts After Listeria Monocytogenes is Detected

FDA, Food, Listeria, Recalls, USDAFDA, USDA

On May 8, 2012, the U.S. Food and Drug Administration (“FDA”) announced the recall of alfalfa sprouts produced by the company Cleveland Beansprouts Co. Discussed here, the Company is recalling the sprouts due to the possible contamination with Listeria monocytogenes. …

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More Recalls of Pet Food in Wake of Salmonella Detection

FDA, Pet Food, Pet foods, Recalls, SalmonellaFDA

The U.S. Food and Drug Administration (“FDA”) has announced the recall of additional pet food due to the detection of Salmonella. According to the FDA, WellPet LLC initiated the voluntary recall as a result of the bacteria being found in …

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FDA Explains its Regulation of Bottled Water

Beverages, Bottled Water, CGMP, FDA, LabelingFDA

Recently, the U.S. Food and Drug Administration (“FDA”) published “Food Facts”, a document providing the public with information concerning the Agency’s regulation of bottled water. Found here, the document details how the Agency works in conjunction with the Environmental Protection …

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FDA Approves New Orphan Drug (Elelyso) to Treat Gaucher Disease

Drugs, FDA, Gaucher disease, Orphan Designation, Orphan DrugFDA

On May 1, 2012, the U.S. Food and Drug Administration (“FDA”) approved a new orphan drug to treat Gaucher disease. The drug, Elelyso (taliglucerase alfa), is an injection therapy used for enzyme replacement in people with the rare genetic disorder. …

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FDA Approves Drug for Treatment of Plague Through Animal Efficacy Rule

Animal Efficacy, Drugs, FDA, Labeling, NDAFDA

On April 27, 2012, the U.S. Food and Drug Administration (“FDA”) approved Levaquin (levofloxacin), a drug used to treat those afflicted with plague. In addition to treating those with the deadly infection, Levaquin is also approved to reduce the risk …

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FDA Warns Companies Marketing Supplements Containing DMAA

Dietary Supplements, Enforcement, FDA, NDI, Supplements, Warning LettersFDA

On April 27, 2012, the U.S. Food and Drug Administration (“FDA”) issued warning letters to several dietary supplement manufacturers in connection with their alleged improper marketing of supplements containing dimethylamylamine (“DMAA”). DMAA, also referred to as geranium extract, is an …

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FDA Approves Vivus Inc.’s Stendra to Treat Erectile Dysfunction

Drugs, Erectile Dysfunction, FDA, NDAFDA

On April 27, 2012, the U.S. Food and Drug Administration (“FDA”) approved the drug Stendra (avanafil), a drug used to treat erectile dysfunction (“ED”). Marketed by Vivus, Inc., Stendra is intended to be taken by men on an as-needed basis …

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FDA Issues Statement on USDA BSE (“mad-cow”) Case

FDA, mad cow, USDAFDA, USDA

On April 26, 2012, the U.S. Food and Drug Administration (“FDA”) issued a statement concerning the recent announcement confirming a case of bovine spongiform encephalopathy (“BSE”). The U.S. Department of Agriculture’s (“USDA”) announcement confirming and explaining this case may be …

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510(k) Adverse Events Allergens Beverages CDRH CGMP Cosmetics Dietary Supplements Disease Claims Drug Drugs Enforcement FDA Food Food Facility Registration Food Safety Modernization Act FSMA FTC Gluten-Free GRAS Guidance imports Injunction Labeling Listeria mad cow Medical Devices NDA Nutrition Facts off-label promotion off-label use Orphan Designation Orphan Drug PMA post-marketing studies Recalls Rulemaking Salmonella Structure-Function Claims Substantiation Tobacco Control Act Tobacco Products Tobacco Warning Letter USDA Warning Letters

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Recent Posts

  • FDA Halts Voluntary Cosmetic Registrations Amidst Overhauls      
  • Congress Increases Minimum Tobacco Sales Age to 21
  • FDA Warns JUUL, Alleging Marketing Violations
  • FDA Warning Letters for Alzheimer’s Supplement Claims
  • FDA Considers Changing Major Food Allergen Labeling Requirements
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