EPA solicits public comment on pesticide residue petitions filed in 2023-2025 for establishment or modification of regulations on various commodities under the Federal Food, Drug, and Cosmetic Act.
Total Nutrition Inc. expands recall of TNVitamins and Doctor's Pride Ultra Potent Complete Green Superfood Moringa Capsules due to potential Salmonella contamination identified during supply chain review.
FDA seeks OMB approval for information collection requirements regarding establishment, maintenance, and availability of traceability records for certain foods under the Paperwork Reduction Act.
FDA submits proposed information collection procedures for safe processing and importing of fish and fishery products to OMB for Paperwork Reduction Act review.
FDA reopens the comment period for its industry guidance on scale-up and postapproval changes for drug dosage forms to allow additional stakeholder input.
FDA extends the comment period for its drug repurposing request for information to allow stakeholders additional time to submit input on addressing unmet medical needs.
Azuma Foods International recalls 545 cases of 3-pack Tako Wasabi seasoned octopus due to undeclared fish allergen that poses serious risk to consumers with fish allergies.
EPA approves Connecticut's State Implementation Plan revision aligning ozone ambient air quality standards with federal requirements and clarifying volatile organic compound calculation methods for adhesive and sealant products.
EPA proposes extending the South Coast air quality nonattainment area's PM2.5 compliance deadline from December 31, 2025, to December 31, 2030; public comment period is 30 days.
FDA classifies Spinal Muscular Atrophy newborn screening test systems as Class II devices, requiring special controls to ensure safety and effectiveness while reducing regulatory burden for manufacturers.
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