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FDA: Press Releases
FDA Approves Vaccines for the 2010-2011 Influenza Season
1 hour 55 min ago
The U.S. Food and Drug Administration announced today that it has approved vaccines for the 2010-2011 influenza season in the United States.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
FDA Statement on the Reopening of Some La. State Waters to Commercial Fishing
4 hours 44 min ago
STATEMENT BY MARGARET A. HAMBURG, COMMISSIONER OF FOOD AND DRUGS, ON THE REOPENING OF SOME LOUISIANA STATE WATERS TO COMMERCIAL FISHING (HR)
Categories: NEWS: U.S. Food and Drug Administration (FDA)
FDA Advisory: Avoid Unintentional Exposure of Children and Pets to Evamist
Thu, 07/29/2010 - 12:59
The U.S. Food and Drug Administration is warning that inadvertent exposure to Evamist through skin contact with patients using this product has the potential for adverse effects in children and pets.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Former CEO of Seafood Importing Corporation Sentenced to Federal Prison for Importing Falsely Labeled Fish
Thu, 07/29/2010 - 10:43
Former CEO of Seafood Importing Corporation Sentenced to Federal Prison for Importing Falsely Labeled Fish
Categories: NEWS: U.S. Food and Drug Administration (FDA)
FDA Approves Drug for Chronic Drooling in Children
Wed, 07/28/2010 - 14:58
The U.S. Food and Drug Administration today approved Cuvposa (glycopyrrolate) Oral Solution to treat chronic severe drooling caused by neurologic disorders in children ages 3 years to 16 years.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
New Early Detection System Helps FDA Identify More than 100 Food Safety Problems in First 7 Months
Wed, 07/28/2010 - 11:01
More than 100 food safety reports were submitted by industry to the U.S. Food and Drug Administration’s new electronic portal in its first months of operation, the agency said today.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Federal Agents Seize FastSize Extenders and FastSize EQM Erectile Quality Monitors
Tue, 07/27/2010 - 15:57
At the request of the U.S. Food and Drug Administration, U.S. Marshals today seized $346,954.43 worth of FastSize Extender devices and FastSize EQM Erectile Quality Monitor devices, as well as component parts used in the manufacture of the FastSize Extender. The FastSize Extender and the FastSize EQM Erectile Quality Monitor are manufactured and distributed by FastSize, LLC of Aliso Viejo, Calif.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Pennsylvania Dairy Farm Agrees to Stop Improper Medication
Tue, 07/27/2010 - 10:43
Owners agree to keep illegal drug residues out of animals sold for human consumption
A Pennsylvania dairy farm has agreed to abide by federal regulations that protect meat from illegal drug residues caused by the unapproved medication of cattle before slaughter, as part of a consent decree of permanent injunction obtained by the U.S. Food and Drug Administration.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
FDA Approves First Generic Enoxaparin Sodium Injection
Fri, 07/23/2010 - 09:45
The U.S. Food and Drug Administration today approved the first generic version of Lovenox (enoxaparin sodium injection), an anti-coagulant drug used to prevent deep vein thrombosis (DVT), a potentially deadly blood clotting condition.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Federal Government Seizes Cyanide Antidote Kits from California Company
Thu, 07/22/2010 - 14:00
At the request of the U.S. Food and Drug Administration, U.S. Marshals today seized $39,000 worth of products labeled as cyanide antidote kits from Keystone Pharmaceuticals in Laguna Hills, California. The seizure warrant was issued by the U.S. District Court for the Central District of California.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
FDA and Other Federal Agencies Collaborate to Improve Chemical Screening
Mon, 07/19/2010 - 11:07
WASHINGTON - The U.S. Environmental Protection Agency (EPA), the National Institute of Environmental Health Sciences National Toxicology Program (NTP) and the National Institute of Health Chemical Genomics Center (NCGC) welcome the U.S. Food and Drug Administration (FDA) to the Tox21 collaboration. The Tox21 collaboration merges federal agency resources (research, funding and testing tools) to develop ways to more effectively predict how chemicals will affect human health and the environment. The collaboration was established in 2008 to develop models that will be able to better predict how chemicals will affect humans. FDA will provide additional expertise and chemical safety information to improve current chemical testing methods.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
New Jersey Woman Sentenced for Committing Insurance Fraud and Selling Prescription Fertility Drugs via the Internet
Mon, 07/19/2010 - 10:26
New Jersey Woman Sentenced for Committing Insurance Fraud and Selling Prescription Fertility Drugs via the Internet
Categories: NEWS: U.S. Food and Drug Administration (FDA)
FDA Warns Consumers, Pharmacists, and Wholesalers Not to Use Stolen Advair Diskus Inhalers
Fri, 07/16/2010 - 12:30
The FDA is warning the public that certain Advair Diskus inhalers stolen from a distribution warehouse in 2009 have been found in some pharmacies. The safety and effectiveness of the stolen inhalers cannot be assured and they should not be used.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
FDA Issues Requirements for Baxter Healthcare Infusion Pump Recall
Tue, 07/13/2010 - 12:47
The U.S. Food and Drug Administration today required Baxter Healthcare Corp. to take specific steps to carry out the April 2010 recall of all Colleague Volumetric Infusion Pumps (CVIP) and to provide customers with a refund, a replacement pump, or lease termination.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Spanish: Federal Agents Seize Bee-Shield Hand Sanitizer from Puerto Rican Company
Mon, 07/12/2010 - 10:15
Los agentes federales decomisan productos desinfectantes para manos Bee-Shield fabricados por una compañía de Puerto Rico
La FDA señala que el gel desinfectante para manos de Bee International Distributors es un medicamento nuevo no autorizado.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Federal Agents Seize Bee-Shield Hand Sanitizer from Puerto Rican Company
Fri, 07/09/2010 - 10:47
At the request of the U.S. Food and Drug Administration, on Thursday, July 8, U.S. Marshals seized $230,000 worth of hand sanitizing gel made by Puerto Rico Beverage Inc. of Maunabo and distributed by Lord Pharmaceutical, LLC, doing business as Bee International Distributors. The hand sanitizer is distributed only in Puerto Rico.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
FDA: New Final Rule to Ensure Egg Safety, Reduce Salmonella Illnesses Goes Into Effect
Fri, 07/09/2010 - 09:23
The U.S. Food and Drug Administration says that as many as 79,000 illnesses and 30 deaths due to consumption of eggs contaminated with the bacterium Salmonella Enteritidis may be avoided each year with new food safety requirements for large-scale egg producers.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Chinese: FDA Public Health Alert: Que She Weight Loss Capsules Contain Potentially Harmful Ingredients
Thu, 07/08/2010 - 13:37
美国食品药物管理局今日发出警告,作为草本减肥补充剂上市的 Que She 含有未列示于产品标签上的活性药物组分,其可能对消费者,特别是对那些患心血管疾病的消费者构成危害。
Categories: NEWS: U.S. Food and Drug Administration (FDA)
FDA Public Health Alert: Que She Weight Loss Capsules Contain Potentially Harmful Ingredients
Thu, 07/08/2010 - 13:05
The U.S. Food and Drug Administration today warned that Que She, marketed as an herbal weight loss supplement, contains active pharmaceutical ingredients not listed on the product label that could harm consumers, especially those with cardiovascular conditions.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
FDA Warns of Risks with Unapproved Use of Malaria Drug Qualaquin
Thu, 07/08/2010 - 09:45
The U.S. Food and Drug Administration today warned that the unapproved use of the malaria drug Qualaquin (quinine sulfate) to treat night time leg cramps has resulted in serious side effects and prompted the manufacturer to develop a risk management plan aimed at educating health care professionals and patients about the potential risks.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
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