FDA Warning Letter to Citra100mg for Unapproved Opioid Sales

The FDA issued a warning letter to Citra100mg for unlawfully selling unapproved and misbranded opioid drugs, including tramadol, to U.S. consumers over the internet. The agency cited violations of the Federal Food, Drug, and Cosmetic Act and highlighted the public health risks associated with unapproved opioids.

AG Tong Joins Coalition Challenging HUD Fair Housing Actions

Connecticut Attorney General William Tong joined 16 other state attorneys general in filing a lawsuit against the Department of Housing and Urban Development (HUD). The lawsuit challenges HUD's actions that threaten to withhold funding from state and local fair housing enforcement agencies for adhering to state laws and for imposing illegal conditions on HUD funding.

CT AG Announces Solar Industry Enforcement and Settlements

Connecticut Attorney General William Tong announced an investigation into SunStrong Management LLC and a $100,000 settlement with Spruce Power 3, LLC. These actions address numerous consumer complaints regarding solar industry companies failing to uphold warranties, manage contracts, and provide adequate customer service.

Florida AG Announces 100 Charges Against CSAM Predator

Florida Attorney General James Uthmeier announced the arrest of Blake McKinniss, who faces 100 criminal charges related to child sexual abuse material (CSAM), including AI-generated content. The investigation was initiated by a cyber tip from the National Center for Missing and Exploited Children.

Navitas KY Alternative Rate Filing Information Request

The Kentucky Public Service Commission has issued a second request for information to Navitas KY NG, LLC regarding its alternative rate filing. Navitas KY is required to provide detailed information on cost allocation factors and gas purchase expense drivers by April 10, 2026.

NYSE Arca Fee Schedule Proposal - Broker Credits

NYSE Arca has proposed amendments to its fee schedule, specifically waiving certain broker credits that were set to expire in March 2026. This filing initiates a public comment period for the proposed changes to the exchange's pricing structure.

NYSE Arca Equities Market Data Fees Amendment Proposal

The NYSE Arca has proposed an amendment to its market data fees, specifically concerning the fees for Consolidated Audit Trail (CAT) data. This proposal outlines new fees for CAT data access and related services, with a comment period open until January 15, 2026.

NYSE American LLC Proposes Market Data Fee Amendments

NYSE American LLC has filed a proposed rule change to amend its market data fees. The filing includes proposed changes to the fees for various data products and services, with a comment period open until February 12, 2026. This action is subject to SEC review.

NYSE American Options Fee Schedule Amendment Proposal

The NYSE American has proposed amendments to its Options Fee Schedule. This filing initiates a public comment period, allowing stakeholders to review and respond to the proposed changes regarding options trading fees.

NYSE Arca Proposes Rule Change for Fees and Charges

NYSE Arca has filed a proposed rule change with the SEC to introduce the NYSE Arca Equity Membership On-Ramp Program. This program offers discounted fees for new Equity Permit Holders for up to 18 months to encourage participation from smaller, retail-oriented market participants. The rule change is proposed to be effective March 6, 2026.

OFAC Adds Persons to SDN List and Updates Identifying Information

The Office of Foreign Assets Control (OFAC) has added new individuals to the Specially Designated Nationals (SDN) List and updated identifying information for an existing SDN. These designations block all property and interests in property subject to U.S. jurisdiction and prohibit U.S. persons from engaging in transactions with the listed individuals.

Civil Rights Commission: South Carolina Advisory Committee Public Meeting Notice

The U.S. Commission on Civil Rights has issued a notice for a virtual business meeting of the South Carolina Advisory Committee. The committee will discuss and potentially vote on a draft project proposal regarding occupational licensing.

PBGC Relaunches Opinion Letter Program for Compliance Assistance

The Pension Benefit Guaranty Corporation (PBGC) has relaunched its Opinion Letter Program to provide compliance assistance. This program allows the public to ask questions about how PBGC would apply laws to specific factual situations, with responses issued by the Office of the General Counsel.

DOT Cracks Down on Illinois DOT Mismanagement of CTA System

The U.S. Department of Transportation's Federal Transit Administration (FTA) has launched a Safety Management Inspection and issued a Special Directive for the Illinois Department of Transportation (IDOT). This action addresses IDOT's alleged mismanagement and failure to properly oversee the safety of the Chicago Transit Authority (CTA) rail transit system.

State v. Flores-Reyes - Montana Supreme Court Ruling

The Montana Supreme Court reversed and remanded the State v. Flores-Reyes case, ruling that evidence discovered during a warrantless search of a vehicle was the fruit of an unconstitutional search. The court's decision addresses the constitutionality of the search, which was dispositive of the appeal.

State v. N. Cole - Montana Supreme Court DUI Affirmation

The Montana Supreme Court affirmed the State v. N. Cole case, concerning a DUI conviction. The court addressed whether the District Court legally imposed a mandatory $5,000 fine when it suspended a portion of it due to the defendant's inability to pay.

State v. Valenzuela - Criminal Appeal

The Montana Supreme Court issued a non-precedential memorandum opinion in State v. Valenzuela, remanding the case with a minor adjustment to street time credit. The court affirmed the district court's disposition with the exception of four additional days awarded to the defendant.

State v. A. Emmings - Criminal Appeal

The Montana Supreme Court has reversed and remanded the case of State v. A. Emmings. The appeal, identified by docket number DA 25-0131, was a direct appeal. The court's decision means the case will be sent back to a lower court for further proceedings.

State v. Larson - Montana Supreme Court Affirmation

The Montana Supreme Court affirmed the District Court's denial of Andrew Larson's motion to dismiss for lack of speedy trial. The case involved charges including DUI, criminal endangerment, and theft following a high-speed chase.

M.A.I.D. v. State - Montana Supreme Court Ruling

The Montana Supreme Court vacated, reversed, and affirmed parts of a District Court's judgment in the case M.A.I.D. v. State. The ruling addresses declaratory judgment and summary judgment on multiple counts, impacting the legal standing and outcomes of the case.

Maleky v. Ohio State Univ. - Court of Claims Remand Scope

The Ohio Court of Appeals affirmed a lower court's decision regarding the scope of a remand in the Maleky v. Ohio State University case. The court found that the Court of Claims did not exceed its remand authority and that certain claims were barred by res judicata.

Galoski v. MedVet Assocs., L.L.C. - Veterinary Malpractice Case

The Ohio Court of Appeals affirmed a lower court's decision granting summary judgment to MedVet Associates, LLC in a veterinary malpractice case. The court found that the veterinary facility itself could not be directly liable for malpractice as the claims sounded in veterinary malpractice and individual veterinarians were not named as defendants.

Peters v. Lawson - Habeas Corpus Petition

The Ohio Court of Appeals dismissed a habeas corpus petition filed by Teresa Peters on behalf of her brother, David Peters. The court found that Teresa Peters failed to demonstrate the necessary conditions to litigate on her brother's behalf.

Order Denying Motion for Sentence Reduction

The Delaware Superior Court denied Tavion Washington's motion for sentence reduction, finding it was filed outside the 90-day window and lacked extraordinary circumstances. The court cited Superior Court Criminal Rule 35(b) as the basis for the denial.

Diamonte Taylor's Motions for Sentence Correction Denied

The Delaware Superior Court denied Diamonte Taylor's motions for sentence correction and appointment of counsel. The court found that Taylor's sentence, which included a 15-year minimum mandatory term for second-degree murder, was consistent with the plea agreement and sentencing recommendations.

State of Delaware v. Joshua Chattin - Compassionate Release Application Denied

The Delaware Superior Court summarily denied Joshua Chattin's application for compassionate release. The denial was based on Chattin's failure to meet the statutory requirements under 11 Del. C. § 4217, including the lack of a required statement from the Department of Corrections and not meeting the age or sentence length criteria.

Delaware Superior Court Denies Sentence Reduction Motion

The Delaware Superior Court denied Mateem Brown's motion for a sentence reduction. The court considered the motion under Criminal Rule 35(b) and found no grounds to alter the previously imposed sentence, which included a total of four years of unsuspended Level V time.

Kilroy v. Popescu - Opinion and Order on Motions

The Delaware Superior Court issued an Opinion and Order ruling on various motions in limine and a motion for summary judgment in the medical negligence case Kilroy v. Popescu. The court addressed disputes regarding the admissibility of evidence and the viability of claims related to a patient's death following a delayed cardiac catheterization.

FDA CDER Response Letter to Hyman, Phelps & McNamara

The FDA's Center for Drug Evaluation and Research (CDER) has posted a response letter addressed to the law firm Hyman, Phelps & McNamara, P.C. The document was made available on March 17, 2025, through the Regs.gov portal. No other details regarding the content of the response are provided.

FDA GRAS Notice 1288 Amendment for Steviol Glycosides

The FDA has posted an amendment to GRAS Notice 1288 concerning enzyme-modified steviol glycosides. This notice is from the manufacturer and is part of the Generally Recognized As Safe (GRAS) notification process.

FDA Complaint Document

The FDA has posted a complaint document related to FDA-2026-H-2311-0001. The document is available for review on the Regs.gov platform. No further details on the nature of the complaint or its implications are provided.

FDA Variance Application from Alpha-Omega Services

The FDA has received a variance application from Alpha-Omega Services, Inc. The application pertains to medical device regulations. Further details are available via the provided URL.

FDA Complaint Document

The FDA has posted a complaint document to the Regs.gov portal on March 17, 2026. The document is available for public viewing and download via the provided link.

FDA CDRH Variance Approval Letter for Photon GFX

The FDA's Center for Devices and Radiological Health (CDRH) has issued a variance approval letter to Photon GFX. This notice indicates a specific approval for a medical device variance, though no further details or documents are available for review.

FDA - Blueroot Health Submission on Respiratory and Immune Function

The FDA has received a submission from Blueroot Health regarding their product, Vital Nutrients, Aller-C, which is intended to support healthy respiratory and immune function. This submission is part of the public record available on Regulations.gov.

FDA Submission: Bio Minerals N.V. Biosil Daily Beauty Protein Vanilla

The FDA has received a submission from Bio Minerals N.V. regarding their product, Biosil Daily Beauty Protein Vanilla. This submission is part of the agency's regulatory process for new product information.

Harmony Foods B12 Gummies Docket Information

The FDA has posted docket information for Harmony Foods LLC concerning their Free & Pure Zero Sugar B12 Gummies. This notice provides access to supporting documentation related to the product, as filed with the agency.

FDA Filing: New Chapter Women's 50+ Multivitamin

The FDA has received a filing from New Chapter regarding their Women's 50+ Multivitamin. This filing pertains to a product supporting immune function, cellular energy, and antioxidants for healthy aging. No specific compliance actions or deadlines are indicated in this notice.

FDA Submission for Harmony Foods Magnesium Citrate Gummies

The FDA has received a submission from Harmony Foods LLC regarding their Meijer Magnesium Citrate Gummies. This notice pertains to a product submission and does not contain new regulatory requirements or guidance.

FDA - Harmony Foods LLC. Meijer Fiber Gummies Submission

Harmony Foods LLC. has submitted information regarding their Meijer Fiber Gummies 72ct product to the Food and Drug Administration (FDA). This submission is part of the agency's regulatory process for food products.

FDA - Better Being Co. Solaray StressMag Product Information

The FDA has posted information regarding Better Being Co.'s Solaray StressMag product, which claims to support mood and relaxation. This filing appears to be a notification or informational submission related to a specific product. No new regulations or enforcement actions are detailed.

FDA - Vitanica BreastBlend Claim Review

The FDA has received a submission regarding Vitanica's BreastBlend product, which claims to support healthy breast tissue. This notice indicates the FDA is aware of the product and its claims, but no specific regulatory action or enforcement is detailed in the provided information.

FDA: L-Theanine Powder Supports Relaxation Claim

The FDA has received a submission regarding L-Theanine Powder, specifically from Threshold Enterprises (Source Naturals), for its product that claims to support relaxation and ease everyday stress. This notice indicates a submission for a dietary supplement claim.

FDA Consultation on i-Health Inc. Culturelle Gummies

The FDA has opened a comment period regarding i-Health Inc.'s Culturelle Women's Probiotic + Multivitamin Gummies. This consultation seeks public input on the product, with specific details available via the provided link.

Luxsonix Group Variance Approval Letter

The FDA has issued a variance approval letter to Luxsonix Group. This notice pertains to a specific variance granted by the Center for Devices and Radiological Health (CDRH).

FDA Acknowledgment Letter to Lusonix Group

The FDA has posted an acknowledgment letter sent to Lusonix Group regarding a submission. The letter, authored by CDRH, confirms receipt of materials but provides no further details on the nature of the submission or any regulatory actions.

FDA Document on GreenBio Nutrients Joint Health Capsules

The FDA has posted a document related to GreenBio Nutrients Inc.'s ILEXPOWER and JointAlive Capsules. The document is available for review on the Regs.gov platform. No specific regulatory action or compliance requirement is detailed in the provided information.

FDA Complaint Consultation

The FDA has posted a complaint for public comment, with the comment period closing on March 17, 2026. This action allows stakeholders to provide input on the complaint's content.

FDA Closes Comment Period for Blueroot Health Nutrient Submission

The FDA has closed the public comment period for a nutrient submission from Blueroot Health concerning their B6 + B Complex product. The submission was related to energy metabolism support. No further action is required from the public at this time.

FDA - Swanson Health Products Menopause Support

The FDA has posted a document related to Swanson Health Products' Menopause Support supplement. The document, identified as FDA-2025-S-0024-1968, is available for review on the Regs.gov platform. No specific regulatory action or compliance requirement is detailed in the provided information.