A Kentucky cattle feed manufacturer, a Vermont cheese processing facility, and a New York supplement facility are all on notice from the Food and Drug Administration for violations of federal food safety rules.
The FDA sent the warning letters to the companies in August and September, and posted them for public view in recent days.…
A key plank in the FDA’s platform to slow down the development of antibiotic resistance and extend the life of medications important to humans is in place. The agency announced Wednesday it has completed the implementation of Guidance for Industry #213.
Known in the animal pharmaceutical industry as GFI #213, the Food and Drug…
The U.S. Food and Drug Administration (FDA) contacted two dairies, two seafood processors, and one animal feed processor in its latest round of warning letters to food producers. Shur-Green Farms LLC of Ansonia, OH, was cited for selling adulterated and misbranded animal feed. The farm had misrepresented shipments of Lascadoil — a waste byproduct for…
A trio of food safety and environmental advocacy groups Thursday filed suit against the U.S. Food and Drug Administration, saying the agency has not sufficiently proven that ractopamine, a drug fed to pigs, cattle and turkey, is safe for animals, humans who eat them, or the environment. Ractopamine, a beta-agonist, increases the rate at which …
Brewers are pleased with the revised rules of the Food Safety Modernization Act (FSMA) published last week because their spent grains are now clearly exempted. The byproduct of the brewing process that remains after the mashing and lautering stages is commonly sold or given to farmers to feed to their livestock. Last spring, many…
The U.S. Food and Drug Administration published its revised provisions to four of the Food Safety Modernization Act (FSMA) on Friday morning. Certain aspects of the rules for produce safety, preventive controls for human food, preventive controls for animal food, and Foreign Supplier Verification Programs (FSVP) have been modified to provide more flexibility to producers…
Michael Taylor, the U.S. Food and Drug Administration’s deputy commissioner for foods and veterinary medicine, is trying to calm fears over the fate of human food byproducts – particularly spent grains from breweries – going into animal feed when the Food Safety Modernization Act (FSMA) is fully implemented. “We’ve heard from trade groups and members…
Spent grains have made a lot of headlines in the past couple of weeks. The byproduct of the brewing process that remains after the mashing and lautering stages is commonly sold or given to farmers to feed to their livestock. But brewers have been worried that the Food Safety Modernization Act (FSMA) will impose regulations…
The deadline passed Monday for comments to the U.S. Food and Drug Administration on the preventive controls for animal food rule issued under the Food Safety Modernization Act (FSMA), and the American Feed Industry Association (AFIA) submitted more than 100 pages of comments on what it describes as the most massive overhaul of animal food…
Now that the U.S. Food and Drug Administration will no longer be held to deadlines for FSMA rule comment periods, industry groups are asking for more time to give their input on certain regulations. The National Grain and Feed Association (NGFA), the American Feed Industry Association (AFIA), the Pet Food Institute (PFI) and the National…
According to a safety review conducted by the U.S. Food and Drug Administration, penicillin and tetracycline antibiotic feed additives approved for “nontherapeutic use” do not meet the agency’s current safety standards. In a Natural Resources Defense Council (NRDC) report released today, previously undisclosed FDA documents reveal that none of the 30 products reviewed between 2001…
