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RECALL RECORD — CLASS IIIRecall closedF-1237-2024/FDA enforcement
East West Tea Company, LLC·Dietary Supplements·Mar 12, 2024

Organic Yogi Echinacea Immune Support, Caffeine Herbal Supplement, Serving Size 1 Tea Bag, 16…

What you need to know

Class III

  • What happened

    Organic Yogi Echinacea Immune Support product is recalled because pesticide residues were detected above action levels.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDANationwide (US)More supplements

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameEast West Tea Company, LLC
Recalling firmEast West Tea Company, LLCEugene, OR, United States
UPC / barcodes
0 76950 45010 360 076950 45010 520 076950 45010 7
Lot / date codes
  • Lot #0000184330 Lot #0000184853 Lot #0000185098 Lot #0000185100 Lot #0000185383 Lot #0000185385 Lot #0000185387 Lot #0000185389 Lot #0000185434 Lot #0000185436 Lot #0000185828 Lot #0000185830 Lot #0000185832 Lot #0000186519 Lot #0000186521 Lot #000184062 Lot #0000186900 Lot #0000186902 Lot #0000186904 Lot #0000187357 Lot #0000187359 Lot #0000187400 Lot #0000187402 Lot #0000187769 Lot #0000188028 Lot #0000188030 Lot #0000188045 Lot #0000188114 Lot #0000186600 Lot #0000186910 Lot #0000187155 Lot #0000184691 Lot #0000184963 Lot #0000185381 Lot #0000185518
Distribution area
Nationwide

nationwide

United States

Quantity affectedtotal 54846 packs
Recall initiationFDA report date: May 22, 2024
FDA recall numberF-1237-2024

Beyond the headline

The recall, in context

East West Tea Company, LLC initiated this supplements recall on March 12, 2024. The FDA enforcement report states: Organic Yogi Echinacea Immune Support product is recalled because pesticide residues were detected above action levels. The FDA report lists distribution as: nationwide.

The FDA enforcement report describes the reason as: Organic Yogi Echinacea Immune Support product is recalled because pesticide residues were detected above action levels.

Organic Yogi Echinacea Immune Support, Caffeine Herbal Supplement, Serving Size 1 Tea Bag, 16… was made or distributed by East West Tea Company, LLC in Eugene, OR, United States. This page reflects FDA report F-1237-2024, dated May 22, 2024.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Organic Yogi Echinacea Immune Support, Caffeine Herbal Supplement, Serving Size 1 Tea Bag, 16… recall?

East West Tea Company, LLC recalled Organic Yogi Echinacea Immune Support, Caffeine Herbal Supplement, Serving Size 1 Tea Bag, 16… in an FDA Class III enforcement action reported as F-1237-2024. Organic Yogi Echinacea Immune Support product is recalled because pesticide residues were detected above action levels.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the East West Tea Company, LLC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1237-2024. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.