FDA determines prednisolone tablets 5mg were not withdrawn for safety or effectiveness reasons, allowing continued approval of generic versions meeting regulatory requirements.
FDA classifies foam or gel chemical sterilant/high level disinfectant devices as class II, establishing special controls to ensure safety and effectiveness while reducing regulatory burden.
Revival Animal Health recalls Breeder's Edge Foster Care Canine, Shelter's Choice Canine, and Breeder's Edge Foster Care GM milk replacers due to inconsistent vitamin D levels.
Lehi Valley Trading Company recalls 624 units of 15-ounce High Valley Orchard Chocolate Covered Raisins due to undeclared peanuts posing allergy risk; recall issued June 25, 2026.
Bear Stewart LLC recalls Bakr Brown Butter Chocolate Chunk Ready to Bake Cookie Dough due to undeclared soy that poses serious allergic reaction risk to affected consumers.
FDA received a food additive petition from Sterigenics U.S., LLC proposing ionizing radiation for pathogen reduction in raw enriched wheat flour.
FDA releases VICH Guidance for Industry #110 on anthelmintic effectiveness study design for porcines to standardize international registration requirements for veterinary medicinal products.
FDA releases final guidance on effectiveness study design for canine anthelmintic drugs to standardize data acceptance across national and regional veterinary medicinal product registration requirements.
FDA guidance #109 establishes study design recommendations for anthelmintic drug effectiveness in horses to facilitate universal regulatory acceptance across national and regional markets.
FDA Guidance for Industry #114 provides study design recommendations for anthelmintic drugs in chickens to support universal acceptance of effectiveness data across national and regional veterinary medicinal product requirements.
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