Healthcare & Life Sciences

AMA Applauds Bill Exempting Physicians from H-1B Visa Fee

The American Medical Association (AMA) is applauding the introduction of bipartisan legislation that would exempt physicians and other health care professionals from a $100,000 filing fee on new H-1B visa petitions. This action aims to alleviate costs for hiring medical professionals and address physician shortages.

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 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 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.

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 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 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 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.

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.

Harmony Foods Multivitamin Gummies - FDA Docket

The FDA has opened Docket FDA-2025-S-0024 concerning Harmony Foods Multivitamin Gummies. An attachment from Harmony Foods LLC provides details on their Meijer Wellness Women's Multivitamin Gummies.

FDA Complaint Document

The FDA has posted a complaint document to the Regs.gov portal. The document, authored by CTP, is available for review and download. No specific details regarding the nature of the complaint or its implications are provided in the metadata.

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: 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 Complaint Document

The FDA has posted a complaint document related to FDA-2026-H-2575-0001. The document was made available on March 17, 2026, and is authored by CTP.

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.

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.

Ashley County Health Unit Closure and Service Relocation

The Arkansas Department of Health has announced the temporary closure of the Ashley County Health Unit in Crossett due to storm damage. All services previously offered at the Crossett location have been relocated to the Ashley County Health Unit in Hamburg.

South Carolina Measles Outbreak Update

The South Carolina Department of Public Health reported one new measles case, bringing the total outbreak count to 997. The update also provided data on age breakdown and vaccination status of cases. Vaccination is emphasized as the best prevention method.

Medicare Coverage of Diabetes Supplies

CMS has released a fact sheet detailing Medicare coverage for diabetes supplies under Part B and Part D. The guidance clarifies which supplies and services are covered and which are not, aiming to inform beneficiaries and providers.

Hospital Price Transparency Requirements and Resources Fact Sheet

The Centers for Medicare & Medicaid Services (CMS) has released a fact sheet detailing hospital price transparency requirements. This document outlines the pricing information hospitals must provide and offers resources to assist them in meeting accessibility and file requirements.

Medicare Diabetes Prevention Program Expanded Model Booklet

CMS has released a booklet detailing the Medicare Diabetes Prevention Program Expanded Model. This guidance explains how healthcare providers can enroll as Medicare-enrolled MDPP suppliers to help patients with prediabetes reduce their risk of developing diabetes.

Intravenous Immune Globulin Items, Services, Billing, and Coding

The Centers for Medicare & Medicaid Services (CMS) has released a fact sheet detailing coverage, supplier eligibility, billing, and coding requirements for Intravenous Immune Globulin (IVIG) items and services. This guidance aims to clarify program integrity and claims processing for providers.

CMS IDTF Booklet: Program, Enrollment, and Billing

The Centers for Medicare & Medicaid Services (CMS) has released a new booklet providing an overview of the Independent Diagnostic Testing Facility (IDTF) program. The publication covers program details, enrollment requirements, and billing issues for IDTFs.

ATSDR Seeks Nominations for Toxicological Profile Development Substances

The Agency for Toxic Substances and Disease Registry (ATSDR) is seeking nominations for substances to be evaluated for toxicological profile development. The public comment period for nominations closes on May 18, 2026.

Philips Recalls Allura Xper/Azurion Systems for X-ray Imaging Issues

Health Canada issued a recall for Philips Allura Xper and Azurion X-ray imaging systems due to performance issues with the wired foot switch. The recall affects multiple models and advises healthcare providers to contact the manufacturer for additional information.

Health Canada Recalls Disinfectant Spray & Wipe Cleaner

Health Canada has issued a recall for specific lots of Coastwide CP15 Disinfectant Spray & Wipe Cleaner due to the active ingredient strength not meeting the labelled concentration. Retailers are instructed on the depth of the recall, and consumers are advised on actions to take.

Medical Device Recall: Incorrect Expiration Dates

Health Canada has issued a recall for several medical devices, including the Approach® CTO Micro Wire Guide and various catheter sets, due to incorrect expiration dates on the labelling. The manufacturer, Cook Incorporated, is providing information to healthcare professionals. This recall impacts multiple lot and model numbers.

Health Canada Recalls GEM PAKs for GEM Premier 5000 Due to Errors

Health Canada has issued a recall for GEM PAKs used with the GEM Premier 5000 due to an increased incidence of 'Process Control Solution Not Detected' errors. These errors can lead to GEM PAK ejection and require replacement, potentially delaying patient management.

Siemens RAPIDPoint 500 Blood Gas Systems Recall

Health Canada has issued a Type II recall for Siemens RAPIDPoint 500 Blood Gas Systems due to Measurement Cartridges potentially being exposed to temperatures outside specified storage conditions during transport. This may affect cartridge performance, and affected healthcare providers should contact the manufacturer.

Olympus Medical Cutting Forceps Recalled Due to Jaw Breakage Risk

Health Canada has issued a Type II recall for Olympus Medical PK/PKS/Everest Cutting Forceps due to a risk of jaw breakage during clinical use. The manufacturer identified inadequate supplier welding validation, and customers are requested to return affected products.

NY DOH Statement on Federal Judge's Ruling in AAP v. ACIP Case

The New York State Department of Health issued a statement from Commissioner Dr. James McDonald regarding a federal judge's ruling in the American Academy of Pediatrics v. Advisory Committee on Immunization Practices case. The statement expresses encouragement regarding the acknowledgment of flaws in the Advisory Committee on Immunization Practices and reaffirms the Department's commitment to science-backed vaccine recommendations.

ATSDR Substance Nominations for Toxicological Profiles

The Agency for Toxic Substances and Disease Registry (ATSDR) is seeking public nominations for substances to be evaluated for upcoming toxicological profiles. This notice opens a comment period for interested parties to suggest substances and provide rationale, with comments due by May 18, 2026.

ATSDR Toxicological Profile Public Comment Period

The Agency for Toxic Substances and Disease Registry (ATSDR) is providing a public comment period for its toxicological profiles. Interested parties can submit comments and attachments through the Regulations.gov portal. The deadline for submitting comments is May 18, 2026.

Mississippi Medical Board Orders Action Against Dr. Richard Cook's License

The Mississippi State Board of Medical Licensure has issued a Determination and Order against Dr. Richard Cook, License No. 31126. The action stems from an investigation into a social media post promoting a mobile hydration event and the subsequent complaint filed against the licensee.

John Keith McKelvey, M.D. - Medical Licensure Consent Order

The Mississippi State Board of Medical Licensure has issued a Consent Order with John Keith McKelvey, M.D., regarding his application for permanent medical licensure. The order grants licensure but restricts his practice to occupational medicine due to prior limitations in other jurisdictions related to his medical history.

Mississippi Medical Board - Permanent Medical License Order for Eswara Kumar Mundra, M.D.

The Mississippi State Board of Medical Licensure issued an order regarding the application for a permanent medical license of Eswara Kumar Mundra, M.D. The order addresses the applicant's request for a waiver of certain training and examination requirements.

Sunil Kurup MD License Suspended in Colorado, North Dakota

The Mississippi State Board of Medical Licensure has automatically suspended the Mississippi medical license of Sunil Kurup, MD, due to disciplinary actions in other states, including license suspensions in Colorado and North Dakota. This suspension prohibits Dr. Kurup from practicing medicine in Mississippi.

Fred Adair Blackledge, M.D. surrenders medical license

The Mississippi State Board of Medical Licensure has accepted the voluntary surrender of Dr. Fred Adair Blackledge's medical license, effective December 31, 2025. This action resolves an ongoing investigation into alleged violations of the Mississippi Medical Practice Act.

Salmonella Cases Linked to Dietary Supplement

The Minnesota Department of Health issued a notice warning consumers not to consume Live it Up Super Greens dietary supplement due to a link to Salmonella infections. The product is being voluntarily recalled by the company.

Minnesota Department of Health Encourages Blood Pressure Monitoring

The Minnesota Department of Health (MDH) is encouraging residents to monitor their blood pressure regularly, particularly during American Heart Month. The notice highlights the risks of high blood pressure and provides guidance on self-measured blood pressure monitoring.