FDA amends sunscreen monograph M020 to add bemotrizinol at concentrations up to 6 percent as a generally recognized as safe and effective active ingredient for over-the-counter sunscreen products.
FDA classifies combined acoustic and electrical external stimulation devices for tinnitus relief as Class II medical devices, subject to special controls to ensure safety and effectiveness.
The Commission on Laboratory Accreditation (COLA) receives five-year deeming authority to accredit clinical laboratories in histocompatibility under the Clinical Laboratory Improvement Amendments of 1988.
CMS is seeking public comment for 60 days on proposed information collection activities under the Paperwork Reduction Act of 1995.
CMS invites public comment on proposed information collection activities under the Paperwork Reduction Act; interested parties may submit feedback on burden estimates and collection methodology.
Centers for Medicare & Medicaid Services requests 60-day public comment on proposed information collection activities under the Paperwork Reduction Act.
Clover Hill Dairy voluntarily recalls all Soft Ricotta/Requeson Cheese products due to potential Listeria monocytogenes contamination posing health risks to vulnerable populations.
GO Raw LLC expands its February 17, 2026 recall of Steve's Real Food Freeze-Dried Chicken Recipe to include an additional lot due to potentially low thiamine (Vitamin B1) levels.
FDA determines protamine sulfate intravenous solution (50 mg/5 mL) and related drug products were not withdrawn for safety or effectiveness reasons, permitting continued ANDA approvals for equivalent formulations.
Nelson & Isa Lacteos LLC recalls 1-pound packages of Requeson Cheese due to potential Listeria monocytogenes contamination posing serious health risks to vulnerable populations.
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