Get The Tea Life Change Fat Burner Contains Soy - Recall Notice
Get The Tea recalls Life Change Fat Burner capsules due to soy content. This product contains soy, which may pose health risks for some consumers.
Lower-risk recall
Get The Tea is notifying customers that Life Change Fat Burners contain soy.
Contact the company
What happened, in plain English
Get The Tea is recalling Life Change Fat Burner capsules because they contain soy. This could be a concern for individuals with soy allergies or sensitivities. Read more at govinfonow.com/recall/19629-get-the-tea-life-change-fat-burner-contains-soy-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/19629-get-the-tea-life-change-fat-burner-contains-soy-recall · Updated October 7, 2026 · FDA enforcement record: FDA #F-0880-2018
Cite this page
“Get The Tea Life Change Fat Burner Contains Soy - Recall Notice.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19629-get-the-tea-life-change-fat-burner-contains-soy-recall. Based on FDA recall #F-0880-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0880-2018%22&limit=1).
Why it’s dangerous
The product contains soy, which can cause allergic reactions in sensitive individuals. Soy allergies may lead to symptoms like hives, swelling, or difficulty breathing in severe cases.
Who’s affected
People who have purchased the Life Change Fat Burner capsules are likely affected. Those with soy allergies or sensitivities are at higher risk.
How to tell if you have this one
Check for the product name 'Life Change Fat Burner' with 90 gel capsules. The product was sold with a 1000mg dose and taken twice daily.
- Brand
Get The Tea- Category
Food
What to do — step by step
Check Product Label
Look for the product name 'Life Change Fat Burner' with 90 gel capsules and 1000mg per capsule.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “100% internet customers nationwide and worldwide. No govt/VA/military consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 5 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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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-0880-2018 (February 23, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0880-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.