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.

Today, as part of the Trump Administration’s ongoing commitment to accelerating lifesaving medical innovations for Ameri...
09/04/2026

Today, as part of the Trump Administration’s ongoing commitment to accelerating lifesaving medical innovations for American patients, we granted accelerated approval to an estrogen receptor antagonist in combination with a CDK4/6 inhibitor for adults with HR+/HER2- locally advanced or metastatic breast cancer with an ESR1 mutation. This expands treatment options for women with advanced breast cancer.

https://www.fda.gov/news-events/press-announcements/fda-grants-accelerated-approval-new-breast-cancer-treatment

Recall expansion: Do not eat, sell, or serve a specific lot of recalled Great Value frozen berries or recalled GreenWise...
09/03/2026

Recall expansion: Do not eat, sell, or serve a specific lot of recalled Great Value frozen berries or recalled GreenWise frozen berries.

See the updated advisory for additional products. https://www.fda.gov/food/outbreaks-foodborne-illness/outbreak-investigation-e-coli-o145h28-frozen-blueberries-july-2026

Do not eat, sell, or serve, recalled GreenWise-brand Organic Frozen Whole Blueberries or Whole Mixed berries. See the advisory for additional information. FDA’s investigation is ongoing. https://www.fda.gov/food/outbreaks-foodborne-illness/outbreak-investigation-e-coli-o145h28-frozen-blueberries-july-2026

Today, the FDA issued an Emergency Use Authorization for Capstar (Nitenpyram) tablets and has revised the authorization ...
09/03/2026

Today, the FDA issued an Emergency Use Authorization for Capstar (Nitenpyram) tablets and has revised the authorization for generic Nitenpyram tablets.

Both products are authorized for the prevention and treatment of New World screwworm infestations in dogs, puppies, cats, and kittens that weigh at least two pounds and are at least four weeks old.

Most U.S. pets remain at low risk.

Learn more: https://www.fda.gov/news-events/press-announcements/fda-issues-emergency-use-authorization-drugs-prevent-and-treat-new-world-screwworm-dogs-and-cats

The FDA is actively working with all six manufacturers of estradiol transdermal patches to increase supply amid growing ...
09/03/2026

The FDA is actively working with all six manufacturers of estradiol transdermal patches to increase supply amid growing demand.

While patches remain available, availability may vary by product, pharmacy or location.

If you’re having trouble finding your usual patch:

Ask your pharmacist about availability or another FDA-approved patch that may be appropriate.

Talk with your healthcare provider about available treatment options.

Do not stop or change your medication without first talking with your healthcare provider.

Check back with your pharmacy, as availability may change as additional supply becomes available.

FDA continues to closely monitor supply and work with manufacturers to support patient access.

Learn more: https://www.fda.gov/drugs/drug-alerts-and-statements/fda-update-estradiol-transdermal-patch-availability

Have you heard about PFAS in medical devices? Here's what you need to know. The FDA has issued FAQs to help patients bet...
09/01/2026

Have you heard about PFAS in medical devices? Here's what you need to know.
The FDA has issued FAQs to help patients better understand PFAS — a group of man-made chemicals — and how they're used in certain medical devices.
Here are the key takeaways:

*Not all PFAS are the same. The type of fluoropolymers (a category of PFAS) used in medical devices are different from the ones linked to health concerns in other settings, like in the environment or consumer products.
*These materials are critical parts of life-saving medical devices like catheters, heart implants, and wound dressings. In many cases, there's no substitute that works as well.
*The FDA is committed to protecting the public health.

Want to learn more? Visit the FDA's updated webpage on PFAS in medical devices.

https://www.fda.gov/medical-devices/products-and-medical-procedures/pfas-medical-devices-what-you-need-know

Recall Expansion: Do not eat, sell, or serve recalled sprouts. FDA’s investigation is ongoing. For more information refe...
08/31/2026

Recall Expansion: Do not eat, sell, or serve recalled sprouts. FDA’s investigation is ongoing.

For more information refer to the outbreak advisory. https://www.fda.gov/food/outbreaks-foodborne-illness/outbreak-investigation-shiga-toxin-producing-e-coli-salmonella-sprouts-august-2026

Do not eat, sell, or serve, Calco and Everything Sprouts-brand alfalfa sprouts. FDA’s investigation is ongoing. See the advisory for additional information. https://www.fda.gov/food/outbreaks-foodborne-illness/outbreak-investigation-shiga-toxin-producing-e-coli-salmonella-sprouts-august-2026

08/31/2026

, this one’s for you!

The FDA Office of Women's Health wants to help you make your health a priority this semester. Whether you’re looking for tips on mental health, nutrition, medications or other health topics, we have free resources designed just for you — and they’re free!
Explore our webpage today: www.fda.gov/collegewomen

Looking for FREE materials to support adults who smoke on their journey to quit ci******es for good? You can request smo...
08/28/2026

Looking for FREE materials to support adults who smoke on their journey to quit ci******es for good? You can request smoking cessation education posters and other materials here: https://digitalmedia.hhs.gov/tobacco/

Important Notice for Mammography Center of Monterey Patients:If you received a mammogram at the Mammography Center of Mo...
08/28/2026

Important Notice for Mammography Center of Monterey Patients:

If you received a mammogram at the Mammography Center of Monterey in California on or after December 22, 2023, the FDA wants you to know that the facility has not complied with an order to notify patients about possible problems with the quality of their mammograms.
Talk to your healthcare provider, and learn more about FDA's Safety Notification and what steps you may want to take: https://www.fda.gov/radiation-emitting-products/mqsa-reports-and-safety-notifications/mammography-problems-mammography-center-monterey-monterey-california-fda-safety-notification

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