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Stop using now Food recall · FDA · Published April 24, 2019

AmeriHerb Recalls Mullein Leaf Due to E. coli Risk

AmeriHerb International Inc recalls 144 lbs of Mullein leaf c/s potentially contaminated with generic E. coli. Check your product details.

🇺🇸 FDA recall #F-1386-2019FoodAmeriHerb ›
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Recalling firmAmeriHerb International Inc803 E Lincoln Way · Ames, IA 50010-6524
✎ GovInfoNow plain-language explainer

AmeriHerb International Inc is recalling Mullein leaf c/s (Verbascum Thapsus) because the dried spice and herb products may be contaminated with generic E. coli. The recall affects approximately 144 lbs of product packaged in 1 lb plastic bags. No specific remedy or return instructions are provided in this record. Read more at govinfonow.com/recall/17544-ameriherb-recalls-mullein-leaf-due-to-e-coli-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/17544-ameriherb-recalls-mullein-leaf-due-to-e-coli-risk · Updated October 11, 2026 · FDA enforcement record: FDA #F-1386-2019

Cite this page

“AmeriHerb Recalls Mullein Leaf Due to E. coli Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/17544-ameriherb-recalls-mullein-leaf-due-to-e-coli-risk. Based on FDA recall #F-1386-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1386-2019%22&limit=1).

The FDA announced on April 24, 2019, that AmeriHerb International Inc voluntarily recalled Mullein leaf c/s potentially contaminated with generic E. coli. The recall affects 144 lbs of product distributed nationwide and to Canada.

How to tell if you have it

  • Brand: AmeriHerb
  • Product: Mullein Leaf C/S, Verbascum Thapsus
  • Lot code: L-40575
  • Packaging: 1 lb plastic bags
  • Quantity: 144 lbs

The hazard

The dried spice and herb products are potentially contaminated with generic E. coli.

Context

GovInfoNow's records show other recent recalls of similar products include Todd's Seeds Recalls Salad Sprouting Mix for E. coli Risk (2026-09-11) and LEASA Alfalfa Sprouts Recalled Due to E. coli Risk (2026-09-04). Lotus Vaping Monarch Premium Kratom Green Maeng Da Powder Recall: Salmonella Risk occurred on 2025-10-30.

How to tell if you have this one

Look for Mullein leaf c/s (Verbascum Thapsus) in 1 lb plastic bags. The net weight is 1# Net, the lot number is L-40575, and it was manufactured by AmeriHerb LLC in Ames, IA.

  • Brand
    AmeriHerb
  • Category
    Food
FDA recall event · 6 products

All 6 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Customers nationwide (including Puerto Rico). Foreign distribution to Canada.
Recall numberProduct, codes & lotsQuantity
F-1383-2019Parsley flakes, Petroselinum sativum, 1# Net, AmeriHerb LLC, Ames, IA packaged in 1 lb plastic bags; L-40377256 lbs
F-1384-2019Blessed thistle herb c/s, Centaurea benedicus, Not for use during pregnancy, 1# Net, AmeriHerb LLC, Ames, IA packaged in 1 lb plastic bags; L-40376108 lbs
F-1385-2019Dill weed c/s, Anethum graveolens, 1# Net, AmeriHerb LLC, Ames, IA packaged in 1 lb plastic bags; L-405771 lb
F-1386-2019Mullein leaf c/s, Verbascum Thapsus, 1# Net, AmeriHerb LLC, Ames, IA packaged in 1 lb plastic bags; L-40575144 lbs
F-1387-2019Lemon balm leaf c/s, Melissa officinalis, 1# Net, AmeriHerb LLC, Ames, IA packaged in 1 lb plastic bags; L-40228103 lbs
F-1388-2019Goldenseal herb c/s, Hydrastis Canadensis, Not for use during pregnancy, 1# Net, AmeriHerb LLC, Ames, IA packaged in 1 lb plastic bags; L-4042836 lbs
Based on the official FDA remedy

What to do — step by step

  1. Stop using the product

    Do not consume or use the Mullein leaf c/s due to the potential E. coli contamination.

  2. Check your inventory

    Verify if you have the recalled item by checking for lot number L-40575 and 1 lb plastic bag packaging.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFLPuerto Rico: yesPR

FDA distribution: “Customers nationwide (including Puerto Rico). Foreign distribution to Canada.” 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 49 days after the firm started it.

1. Firm started the recall: Apr 24, 201912. FDA classified it Class II: May 16, 201923. Published in FDA’s Enforcement Report: May 22, 201934. FDA terminated the recall: Jun 12, 201942019
  1. Firm started the recall
  2. FDA classified it Class II
  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-1386-2019 (April 24, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1386-2019 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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