The products contain Coltsfoot, which is not to be used internally.
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Contact the company
📍Recalling firmGreen Water, LLC25797 Conifer Rd Unit B102 · Conifer, CO 80433-9053
✎ GovInfoNow plain-language explainer
Green Water, LLC is recalling Taspen's Organics Respiratory Tea sold in 2 oz packages because the product contains Coltsfoot, which is not safe for internal use. The recall covers specific lots with expiration dates ranging from January 2020 to October 2024. Consumers who purchased this tea should check their packaging against the recalled lot numbers. Read more at govinfonow.com/recall/16480-taspen-s-organics-respiratory-tea-recall-coltsfoot-hazard.
“Taspen's Organics Respiratory Tea Recall: Coltsfoot Hazard.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/16480-taspen-s-organics-respiratory-tea-recall-coltsfoot-hazard. Based on FDA recall #F-0709-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0709-2020%22&limit=1).
The FDA announced on Oct. 24, 2019, that Green Water, LLC voluntarily recalled Taspen's Organics Respiratory Tea sold in 2 oz packages due to the presence of Coltsfoot, which is unsafe for internal use.
How to tell if you have it
Brand: Taspen's Organics
Product: Respiratory Tea
Size: 2 oz packages
Lot numbers: 1001 - 1189
Expiration dates: 01/2020-10/2024
Units affected: 69
The hazard
The products contain Coltsfoot, which is not to be used internally. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Green Water, LLC had one other recall on record since July 30, 2019, involving Taspen's Organics Herbal Tinctures with potential Salmonella risk. Other recent recalls of similar products include Wild Coast Brew Tart Chocolaty Tisane Recall (June 5, 2026), Wild Coast Brew Winter Spice Black Tea Recall (June 5, 2026), and Wild Coast Brew Ginger Lemongr: Ashwagandha Tea Safety Recall (June 5, 2026).
How to tell if you have this one
Look for Taspen's Organics Respiratory Tea in 2 oz packages. Check the label for lot numbers between 1001 and 1189. The expiration dates on these packages range from 01/2020 to 10/2024.
Brand
Taspen's Organics
Category
Food
FDA recall event · 3 products
All 3 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
CO, GA, IA, KY physical locations. Nationwide via internet.
Recall number
Product, codes & lots
Quantity
F-0707-2020
Taspen's Organics Breathe Easy Herbal Tincture Dietary Supplement, sold in 1 oz, 2 oz, and 4 oz amber glass bottles with dropper.; Lot numbers 1001 - 1254 Exp: 01/2020-10/2024
197 units
F-0708-2020
Dragonfly Botanicals Full spectrum Breathe Deep 1000mg/oz Dietary Supplement, sold in 0.5 oz, 1 oz, 2 oz, and 4 oz amber glass bottles with dropper.; Lot numbers 1093 and 1108 Exp: 01/2020-10/2024
268 units
F-0709-2020
Taspen's Organics Respiratory Tea, sold in 2 oz packages; Lot numbers 1001 - 1189 Exp: 01/2020-10/2024
69 units
Based on the official FDA remedy
What to do — step by step
Stop consuming the tea
Do not drink the recalled Taspen's Organics Respiratory Tea because it contains Coltsfoot which is not for internal use.
Check your lot numbers
Verify if your package has a lot number between 1001 and 1189 with an expiration date from 01/2020 to 10/2024.
Contact the manufacturer
Reach out to Green Water, LLC for further instructions on how to handle the recalled product.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 4 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “CO, GA, IA, KY physical locations. Nationwide via internet.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Colorado, Georgia, Iowa, Kentucky.
Recall timeline
FDA terminated this recall 19 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0709-2020 (October 24, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0709-2020 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.