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 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 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.
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.
FDA seeks OMB approval for information collection requirements regarding establishment, maintenance, and availability of traceability records for certain foods under the Paperwork Reduction Act.
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.
Department of Labor corrects Form LM-2 Long Form Instructions published June 1, 2026, with missing pages and formatting errors; corrected versions available on the OLMS website.
OSHA expands recognition of TÜV SÜD America, Inc. as a Nationally Recognized Testing Laboratory, broadening its scope for product safety testing and certification services.
FDA classifies simple point-of-care SARS-CoV-2 detection devices as Class II medical devices, requiring special controls to ensure safety and effectiveness while reducing regulatory burden for manufacturers.
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