U.S. FDA Add us as a preferred source on Google

X @us_fda 📍 United States

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🔄 Data last refreshed 1 month ago

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Make a deal with U.S. FDA

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Followers

591.7K

Posts

22.4K

Following

103

Account age

15 yrs

🎁 Free analysisfor U.S. FDA

🕵️Fake Followers CheckReal-audience % & bot risk→ 📊Engagement rateBenchmarked vs. peers→ 💰What they chargeFair sponsored-post price→

Known for

Have a device correction or removal? Not sure what’s required when reporting?

FDA’s Medical Device Recalls FAQ covers Part 7 and Part 806 requirements – from what triggers a report to what info must be included.

 https://t.co/et1yoboDt2

42.8K views Have a device correction or removal? Not sure what’s required when reporting? FDA’s Medical Device Recalls FAQ covers Part 7 and Part 806 requirements – from what triggers a report to what info must be included.  https://t.co/et1yoboDt2

Midwest Poultry Services, L.P. is recalling certain shell eggs due to potential Salmonella contamination. The recalled eggs were produced in Texas between June 6–July 3, 2026, with sell by/best by dates of July 20–Aug. 17. Check for carton codes P-1950 or 0840962 with Julian

20.6K views Midwest Poultry Services, L.P. is recalling certain shell eggs due to potential Salmonella contamination. The recalled eggs were produced in Texas between June 6–July 3, 2026, with sell by/best by dates of July 20–Aug. 17. Check for carton codes P-1950 or 0840962 with Julian

Medical Device Manufacturers. Refer to this list of useful information prior to submitting recall information. Here you will find Form 5072 and FAQs specific to medical device recalls.

Using Form 5072 helps ensure your medical device recall submission includes everything FDA

13.5K views Medical Device Manufacturers. Refer to this list of useful information prior to submitting recall information. Here you will find Form 5072 and FAQs specific to medical device recalls. Using Form 5072 helps ensure your medical device recall submission includes everything FDA

BREAKING: FDA licensed the first freeze-dried plasma product for use in the U.S. Ezplaz Freeze Dried Plasma (FDP) provides a new option for transfusion in adults who require plasma and other plasma products are not available. https://t.co/Co44RqZLjj

12.4K views BREAKING: FDA licensed the first freeze-dried plasma product for use in the U.S. Ezplaz Freeze Dried Plasma (FDP) provides a new option for transfusion in adults who require plasma and other plasma products are not available. https://t.co/Co44RqZLjj

📊 Post performance

11.5K

Avg views / post

1.9%

Reach vs followers

Oct 2010

On X since

🔥 Top post: We're getting a new name on X! Starting Aug. 7th, we become @FDA · 5.2M views

📊 Activity & format

Posting cadence

11.9 / week

Posts daily — consistently active for a campaign window.

Content mix

Mostly images

Recent: 0 video · 12 image · 1 text.

Follower / following

5.7K×

Follows 103 back. A strong ratio — an audience that follows them, not a follow-for-follow network.

Recent posts

View on X ↗

🔥 Top post We're getting a new name on X! Starting Aug. 7th, we become @FDA. If you follow us now, you don't have to change a thing to keep following us. New handle, same trusted public health information. 5.2M❤ 314🔁 203

Have a device correction or removal? Not sure what’s required when reporting? FDA’s Medical Device Recalls FAQ covers Part 7 and Part 806 requirements – from what triggers a report to what info must be included.  https://t.co/et1yobo… 42.8K❤ 14🔁 8

Medical Device Manufacturers. Refer to this list of useful information prior to submitting recall information. Here you will find Form 5072 and FAQs specific to medical device recalls. Using Form 5072 helps ensure your medical device re… 13.5K❤ 7🔁 4

Use FDA Form 5072 to ensure your medical device recall submission is complete. FDA is encouraging device manufacturers to consider using FDA Form 5072, “Device Correction and Removal Report,“ when submitting required information for vol… 11.1K❤ 13🔁 8

Join us on Thursday July 30th from 9:30 a.m.–4:50 p.m. ET for a Public Meeting of the Cellular, Tissue, and Gene Therapies Advisory Committee discussing Replimune’s BLA for vusolimogene oderparepvec, in combination with nivolumab, for adva… 11.5K❤ 7🔁 11

BREAKING: FDA licensed the first freeze-dried plasma product for use in the U.S. Ezplaz Freeze Dried Plasma (FDP) provides a new option for transfusion in adults who require plasma and other plasma products are not available. https://t.co/… 12.4K❤ 36🔁 19

Join us on Wednesday July 29 from 9:30 a.m.–4:50 p.m. ET for a Public Meeting of the Cellular, Tissue, and Gene Therapies Advisory Committee discussing Capricor, Inc.’s Biologics License Application for deramiocel (human allogeneic cardios… 10K❤ 16🔁 6

The FDA is seeking patients & caregivers to share their experiences living w/ End-Stage Renal Disease (ESRD) and receiving home hemodialysis during a virtual Patient Listening Session on 9/28 1 pm-2:30 pm ET. To be considered, comple… 8.8K❤ 11🔁 7

👓 Dark lenses ≠ UV protection! When choosing sunglasses, look for a UV400 rating or "100% UV protection" on the label — not just a dark tint. And don't forget the kids — toy sunglasses may offer zero UV protection. Keep those eyes safe thi… 9.9K❤ 19🔁 9

News: Today, the FDA approved SimpleScreen™ CRC (Freenome LLC), a blood test that screens for colorectal cancer in average-risk adults aged 45 years and older, offering a new option that may help more people get screened. https://t.co/0q… 12K❤ 58🔁 27

Midwest Poultry Services, L.P. is recalling certain shell eggs due to potential Salmonella contamination. The recalled eggs were produced in Texas between June 6–July 3, 2026, with sell by/best by dates of July 20–Aug. 17. Check for carton… 20.6K❤ 54🔁 53

NEWS: @US_FDA approves a treatment for ROS1-positive non-small cell lung cancer. https://t.co/sgtRTU4VJ4 8.6K❤ 13🔁 7

💡 Facts

🗓️Joined X in 2010 — 15 years ago.

👁️Averages 11.5K views per post.

📤Posts about 11.9× per week.

💬0.01% engagement rate.

🏅Earned the 100K Followers for passing 100K followers.

📍Based in United States.

🕵️ Fake follower check

Estimated

37/100

Low Credibility score

66%

Mixed Real audience

Medium Fake-follower risk

High Data confidence

Est. 66% real, active audience · Medium fake-follower risk.
Low engagement (~1.9% of followers engage each post) — a sign of an inflated or inactive audience.
Organic base — far more followers than accounts it follows.
Established account (15+ years old).
0.01% engagement — below the ~14.4% typical for this size.

Heuristic estimate from engagement, follower ratios, account age & growth — a screening signal, not a guarantee.

About

Our posts are FDA Approved! Privacy Policy - http://go.usa.gov/xFfG8 FDA Authentic Accounts - http://bit.ly/FDASocial

📸 Gallery

🔀 Audience overlap

Estimated

Estimated shared audience with similar creators — useful for avoiding overlap (or doubling down) when planning a campaign.

Ambassador Tom Rose 33%

OutKick 30%

Concacaf 29%

United Football League 17%

Morph 11%

SavageMike 10%

More like this

Ambassador Tom Rose ✓

United Football League ✓

@theufl

372.2K Followers

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How many followers does U.S. FDA have?

U.S. FDA has 591,664 followers on X.

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