U.S. Food and Drug Administration

U.S. Food and Drug Administration The official page of the U.S. Food and Drug Administration. Our posts are all FDA APPROVED! The U.S. Food and Drug Administration or the federal government.

Food and Drug Administration maintains Facebook, Instagram, Threads, X and other social media accounts to share updates about FDA activities and public-health-related information about FDA-regulated products. The FDA has instituted the following policy regarding comments posted to FDA’s social media accounts:

General Comment Guidelines

To maintain respectful interaction on this page, we encourag

e that all comments:

- Stay focused. All viewpoints are welcome, but comments should be relevant to the specific post under which it appears.
- Be respectful. Respect others’ opinions and share your opinions in a respectful way.
- Tell the truth. Spreading false or misleading information about FDA-regulated products harms the public health.
- No spam. This includes unsolicited commercial messages and a single user’s repeated comments on a topic unrelated to the underlying post. Comment Expectations

Although we hope that you choose to contribute your comments, to protect privacy, please do not disclose personally identifiable information about yourself or other individuals. We welcome your comments and request that you respect the informational resources provided by FDA’s social media accounts. Also, any comments, posts or links that seek to defame, slander or libel any current or former employees (including contractors) of the FDA will be hidden or removed. We will consider your comments when posting new updates, but we may not respond directly to individual inquiries. We are unable to answer questions about your specific health care situation. The FDA does not endorse the comments or opinions provided by visitors to its social media accounts. FDA following users or sharing content does not imply FDA endorsement. We retain the discretion to determine which comments violate our comment policy. We also reserve the right to hide or remove comments and/or disable commenting. The views expressed within posted comments do not necessarily reflect those of the U.S. Comment Moderation

Depending on the platform, comments may be filtered, hidden, and/or removed. We are using these terms to mean the following:

“Filtered” or “filtered and hidden” means that the platform or agency system automatically flagged the comment. It is typically hidden from most users but may still be visible to a limited subset of users.
“Hidden” means that the agency manually flagged the comment to be hidden from most users, but that it may still exist on the platforms in a limited fashion.
“Removed” and “deleted” have the same definition and mean that the agency manually removed the comment from the platform. A record of that removed comment is preserved in accordance with FDA’s Social Media Policy and the Records Retention Schedule. Comments may be automatically filtered and hidden by the social media platform if:

- The comment contains profanity.
- The comment contains an image.
- The comment contains a video.
- The comment contains a link/URL.
- The comment contains keywords from known scam attempts.
- The user does not have a profile picture.
- The user has had their account for one week or less.
- The user does not have any friends or followers.
- The user has had at least three comments reported, deleted, or hidden in the previous 30 days. Comments visible on social media accounts may be hidden or removed by FDA if they:

- Were not hidden despite matching the automated filter criteria as outlined above.
- Appear to be spam, including comments containing commercial endorsements, commercial solicitations, WhatsApp numbers, or a single user’s repeated comments on a topic unrelated to the underlying post.
- Contain discriminatory, racist, offensive, obscene, inflammatory, threatening, or unlawful statements, language, or content.
- Include personally identifiable information for individuals such as email addresses, phone numbers, and mailing addresses.
- Violate the comment policy. Because we want to avoid commercial solicitations and malicious links in our comments, our filters hide comments that contain URLs. To the extent a commenter wishes to reference relevant material available from other sources, please provide a citation or other bibliographic information without including a link. If you think your comment may have been hidden or removed in error, please contact us at [email protected] with details. Records will be kept of all comments that are removed by FDA for the above reasons. We reserve the right to block offenders of this policy.

Happy 50th Anniversary, CDRH!On May 28, 1976, the Medical Device Amendments were signed into law — a landmark moment tha...
05/28/2026

Happy 50th Anniversary, CDRH!

On May 28, 1976, the Medical Device Amendments were signed into law — a landmark moment that transformed how the United States regulates medical devices and protects patients while advancing innovation.

Before 1976, the FDA had limited authority over medical devices. The Medical Device Amendments changed everything by establishing a three-tier classification system (Class I, II, and III) for medical devices, creating the 510(k) and Premarket Approval (PMA) pathways, and empowering the FDA to ensure devices are safe and effective before they reach patients.

The Center for Devices and Radiological Health (CDRH), as we know it today, has worked tirelessly to bring safe, effective, and innovative medical devices to the patients who need them.

Fifty Years of the Medical Device Amendments. Fifty years of protecting patients. Fifty years of innovation.

Here's to the next 50!

https://www.fda.gov/news-events/fda-voices/fifty-years-medical-device-amendments-building-strong-foundation-advance-safe-effective-and-high

FDA is advising consumers not to eat, sell, or distribute recalled moringa powder dietary supplements sold under the Tnv...
05/27/2026

FDA is advising consumers not to eat, sell, or distribute recalled moringa powder dietary supplements sold under the Tnvitamins, Doctor’s Pride, and Mogo brands due to possible Salmonella contamination.

FDA has issued advisories for two Salmonella outbreaks linked to products containing moringa leaf powder.

Check your home and throw these recalled products away.

Learn more:

New Outbreak Advisory for recalled Mogo products: https://www.fda.gov/food/outbreaks-foodborne-illness/outbreak-investigation-salmonella-moringa-leaf-powder-may-2026

Updated Outbreak Advisory for recalled Tnvitamins and Doctor’s Pride products: https://www.fda.gov/food/outbreaks-foodborne-illness/outbreak-investigation-salmonella-moringa-leaf-powder-january-2026

Did you know that   affects women more than men – especially after  . Osteoporosis develops when bone mass and bone mine...
05/27/2026

Did you know that affects women more than men – especially after . Osteoporosis develops when bone mass and bone mineral density decrease, leading to weaker bones and a higher risk of fracture. The good news? There are medicines that can protect your bone health. Learn more from the FDA Office of Women’s Health: https://www.fda.gov/consumers/womens-health-topics/osteoporosis

The FDA authorized marketing of the DeepView AI System, a prescription-only adjunctive diagnostic device intended to aid...
05/26/2026

The FDA authorized marketing of the DeepView AI System, a prescription-only adjunctive diagnostic device intended to aid healthcare provider assessment and care of burn wounds on patients.

This innovative system combines advanced imaging technology with artificial intelligence to help doctors identify areas that may not heal within 21 days, which can inform whether further treatment of the burn is needed.
This authorization is part of the FDA’s ongoing commitment to delivering innovative solutions that support improvements in patient outcomes.

https://www.accessdata.fda.gov/cdrh_docs/pdf25/DEN250028.pdf

  is a chronic  . Rather than fighting infection, the immune system attacks healthy cells, tissues and organs. Women are...
05/26/2026

is a chronic . Rather than fighting infection, the immune system
attacks healthy cells, tissues and organs. Women are disproportionately affected. Use FDA Office of Women’s Health resources to learn the facts about lupus and tips to help manage symptoms:
https://www.fda.gov/consumers/womens-health-topics/lupus-and-women

05/26/2026
05/25/2026

Memorial Day is more than a long weekend. It is a time to remember the heroes who never made it home.

Today, we honor their sacrifice, reflect on the freedoms they fought to protect, and hold close the families who continue to carry their memory forward.

Today, the FDA approved Hepcludex (bulevirtide-gmod) injection, the first FDA-approved treatment for chronic hepatitis d...
05/22/2026

Today, the FDA approved Hepcludex (bulevirtide-gmod) injection, the first FDA-approved treatment for chronic hepatitis delta virus (HDV) infection in adults. This approval fills a critical gap in care for patients who, until now, have had no FDA-approved therapies available to treat this serious and life-threatening condition. https://www.fda.gov/news-events/press-announcements/fda-approves-first-treatment-chronic-hepatitis-delta-virus-hdv-infection

Hepcludex was granted Breakthrough Therapy Designation and Orphan-Drug Designation. Hepcludex also received priority review and was approved under the Accelerated Approval pathway — reflecting the urgency and significance of this milestone.

Today's approval addresses a critical need for people with chronic HDV infection and builds on the FDA's commitment to advancing the health of all Americans.

FDA has approved a new over the counter (OTC) option for people with acne. Differin Epiduo Acne Gel combines two active ...
05/22/2026

FDA has approved a new over the counter (OTC) option for people with acne. Differin Epiduo Acne Gel combines two active ingredients, adapalene (a retinoid) and benzoyl peroxide, in a once-daily gel for adults and teens 12 years and older. Previously available only by prescription, it is now an FDA-approved OTC dual active ingredient acne treatment.

This product will continue to be available by prescription for children 9 through 11 years of age, while the OTC version is labeled for adults and children 12 years and older.

Learn more: http://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&varApplNo=220736

Did you know that a sudden increase in blood pressure during   can be life-threatening for both you and your baby?   is ...
05/22/2026

Did you know that a sudden increase in blood pressure during can be life-threatening for both you and your baby? is serious, especially if you have a history of high blood pressure. Use FDA Office of Women’s Health guide to talk with your health care provider about blood pressure management during pregnancy. https://www.fda.gov/media/147354/download?attachment

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