Skip to content
Food recall · FDA · Published November 17, 2020

Fusion Health and Vitality LLC recalls PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY and IMMUNE HEALTH Dietary Supplement 30 Servings (45g)

Fusion Health is recalling PHARMORIGINS CORE supplements because they contain an unapproved food additive and marketing claims. Stop using if you have the product with specific lot numbers.

🇺🇸 FDA recall #F-0180-2021FoodFusion Health ›
Take action

Contact the company & request your remedy

Recalling firmFusion Health and Vitality LLC1360 Union Hill Rd, 11B · Alpharetta, GA 30004-8433
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

Fusion Health is recalling their Natural Energy and Immune Health dietary supplement due to using an unapproved food additive and making unapproved marketing claims. This could lead to regulatory issues but does not pose a direct health risk to consumers. Read more at govinfonow.com/recall/15018-fusion-health-recalls-natural-energy-supplement-due-to-unapproved-additive.

Source Summary by GovInfoNow · govinfonow.com/recall/15018-fusion-health-recalls-natural-energy-supplement-due-to-unapproved-additive · Updated October 4, 2026 · FDA enforcement record: FDA #F-0180-2021

Cite this page

“Fusion Health Recalls Natural Energy Supplement Due to Unapproved Additive.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/15018-fusion-health-recalls-natural-energy-supplement-due-to-unapproved-additive. Based on FDA recall #F-0180-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0180-2021%22&limit=1).

Why it’s dangerous

The product contains an unapproved food additive and makes unapproved marketing claims. This means the supplement does not meet FDA regulations and could be misleading about its health benefits.

Who’s affected

People who purchased the PHARMORIGINS CORE supplement with specific lot numbers from the list provided. Those most at risk are individuals who have the product and are concerned about regulatory compliance.

How to tell if you have this one

Check the product label for the name 'PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY and IMMUNE HEALTH Dietary Supplement 30 Servings (45g)'. Look for lot numbers: 200313, 200321, 200326, 200402, 200406, 200410, 200414, 200416, 200424, 200501, 200525, 200527, 200604, or 200610.

  • Brand
    Fusion Health
  • Product
    PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY and IMMUNE HEALTH Dietary Supplement 30 Servings (45g)
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the lot numbers listed: 200313, 200321, 200326, 200402, 200406, 200410, 200414, 200416, 200424, 200501, 200525, 200527, 200604, or 200610.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The product contains an unapproved food additive and makes unapproved marketing claims, but it does not pose a direct health risk. However, it may not meet FDA regulations.

What should I do if I have this product?

Check the product label for the lot numbers listed. If you have the product with those lot numbers, you may want to stop using it and contact the manufacturer for further instructions.

How can I get a refund or replacement?

The recall record does not specify a refund or replacement process. Contact the manufacturer directly for assistance.

Take action

Contact Fusion Health

We’ve drafted a message you can send Fusion Health to request your refund or repair — edit it as you like.

Subject: Recall F-0180-2021 — Fusion Health PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY and IMMUNE HEALTH Dietary

Hello,

I own a PHARMORIGINS CORE with Natural Orange Flavor NATURAL ENERGY and IMMUNE HEALTH Dietary Supplement 30 Servings (45g) that is covered by recall F-0180-2021 from Fusion Health.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

Similar recalls

Keep exploring

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

Comments are reviewed before they appear. No links, ads, or personal attacks — those get removed.

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0180-2021 (November 17, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0180-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA