Skip to content
Food recall · FDA · Published April 12, 2021

Indiana Botanic Gardens, Inc recalls Botanic Choice Green Tea Leaf Extract (3:1 Extract), Alcohol Free Liquid Extract, 1 FLOZ., in glass jar with dropper,

Indiana Botanic Gardens recalls Botanic Choice Green Tea Leaf Extract due to incorrect active ingredient listed on product label. Affected items have UPC 70330:200164 and Lot 6102649.

🇺🇸 FDA recall #F-0489-2021FoodIndiana Botanic Gardens ›
Take action

Contact the company & request your remedy

Recalling firmIndiana Botanic Gardens, Inc3401 W 37th Ave · Hobart, IN 46342-1751
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

Indiana Botanic Gardens is recalling Botanic Choice Green Tea Leaf Extract (3:1 Extract) because the product label lists the wrong active ingredient. This could lead to confusion about what's actually in the product. Read more at govinfonow.com/recall/14707-indiana-botanic-gardens-botanic-choice-green-tea-extract-recall-incorrect.

Source Summary by GovInfoNow · govinfonow.com/recall/14707-indiana-botanic-gardens-botanic-choice-green-tea-extract-recall-incorrect · Updated October 4, 2026 · FDA enforcement record: FDA #F-0489-2021

Cite this page

“Indiana Botanic Gardens Botanic Choice Green Tea Extract Recall: Incorrect Labeling.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14707-indiana-botanic-gardens-botanic-choice-green-tea-extract-recall-incorrect. Based on FDA recall #F-0489-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0489-2021%22&limit=1).

Why it’s dangerous

The product label incorrectly lists the active ingredient. This means consumers might not know what they're actually consuming, which could affect their health decisions or product safety.

Who’s affected

Anyone who purchased the Botanic Choice Green Tea Leaf Extract (3:1 Extract) in glass jar with dropper. People using this product for health or dietary purposes may be at risk of incorrect ingredient information.

How to tell if you have this one

Check for the UPC 703308200164 and Lot 6102649 on the glass jar with dropper. The product is an Alcohol Free Liquid Extract, 1 fl oz.

  • Brand
    Indiana Botanic Gardens
  • Product
    Botanic Choice Green Tea Leaf Extract (3:1 Extract), Alcohol Free Liquid Extract, 1 FLOZ., in glass jar with dropper
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the UPC 703308200164 and Lot 6102649 on the glass jar with dropper.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall is due to incorrect labeling, not safety issues. The product may still be safe but the label is wrong.

What should I do if I have this product?

Check the product label for UPC 703308200164 and Lot 6102649. If it matches, contact Indiana Botanic Gardens for more information.

How can I get a replacement?

The recall record does not mention a replacement option.

Take action

Contact Indiana Botanic Gardens

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

Subject: Recall F-0489-2021 — Indiana Botanic Gardens Botanic Choice Green Tea Leaf Extract (3:1 Extract), Alcohol Free Liquid Ex

Hello,

I own a Botanic Choice Green Tea Leaf Extract (3:1 Extract), Alcohol Free Liquid Extract, 1 FLOZ., in glass jar with dropper that is covered by recall F-0489-2021 from Indiana Botanic Gardens.

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-0489-2021 (April 12, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0489-2021 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