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Stop using now Food recall · FDA · Published May 2, 2017

US Deer Antlers Herbal Tea Recall: Botulinum Toxin Contamination Risk

US Deer Antlers Export & Import recalls Herbal Tea Variety 120ml pouches (40 per case) produced between March 1 and April 30, 2:00017, due to potential Clostridium botulinum contamination. Consumers should avoid use.

🇺🇸 FDA recall #F-2249-2017FoodUS Deer Antlers Export & Import ›
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Recalling firmU S Deer Antlers Export & Import1206 S Western Ave · Los Angeles, CA 90006-3108
✎ GovInfoNow plain-language explainer

What happened, in plain English

US Deer Antlers Export & Import is recalling Herbal Tea Variety 120ml pouches (40 per case) produced between March 1 and April 30, 2017, because they may contain Clostridium botulinum, a dangerous bacteria that can cause botulism. This recall is critical as botulism can lead to serious illness or death if consumed. Read more at govinfonow.com/recall/21802-us-deer-antlers-herbal-tea-recall-botulinum-toxin-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/21802-us-deer-antlers-herbal-tea-recall-botulinum-toxin-contamination-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-2249-2017

Cite this page

“US Deer Antlers Herbal Tea Recall: Botulinum Toxin Contamination Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21802-us-deer-antlers-herbal-tea-recall-botulinum-toxin-contamination-risk. Based on FDA recall #F-2249-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2249-2017%22&limit=1).

Why it’s dangerous

Clostridium botulinum is a bacterium that produces a potent neurotoxin. If the bacteria grow in the tea during storage, it can cause botulism, a rare but life-threatening illness that affects the nervous system and can lead to paralysis or death.

Who’s affected

Anyone who purchased Herbal Tea Variety 120ml pouches (40 per case) from US Deer Antlers Export & Import between March 1 and April 30, 2017. People who have consumed the product are at highest risk of botulism.

How to tell if you have this one

Check for Herbal Tea Variety 120ml pouches (40 per case) with production dates between March 1 and April 30, 2017. The product was manufactured at the company's premises during this period.

  • Brand
    US Deer Antlers Export & Import
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Now

    Immediately stop using and discard any Herbal Tea Variety 120ml pouches (40 per case) produced between March 1 and April 30, 2017.

Where it went and when

Where it was distributed

Distributed in 14 states, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: yesNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: not listedFL

FDA distribution: “US: CA, TX, NC, NY, VA, HI, GA, WA, IL, PA, OK, MO, MD, NJ. Korea.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Georgia, Hawaii, Illinois, Maryland, Missouri, New Jersey, New York, North Carolina, Oklahoma, Pennsylvania, Texas, Virginia, Washington.

Recall timeline

FDA terminated this recall 43 days after the firm started it.

1. Firm started the recall: May 2, 201712. FDA classified it Class I: May 24, 201723. Published in FDA’s Enforcement Report: May 31, 201734. FDA terminated the recall: Jun 14, 201742017
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. 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-2249-2017 (May 2, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2249-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 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