Food recall

Green Water, LLC recall: Taspen's Organics Breathe Easy Herbal Tincture Dietary Supplement

Green Water, LLC, of Conifer, CO, recalled Taspen's Organics Breathe Easy Herbal Tincture Dietary Supplement and 2 other products. The FDA's reason: “The products contain Coltsfoot, which is not to be used internally.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on October 24, 2019, and the FDA first listed it in its Enforcement Report of February 26, 2020. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

See FDA's words below

Status

Terminated

Closed June 7, 2021

The recall

Company
Green Water, LLC (Conifer, CO)
Reason, in FDA's words
“The products contain Coltsfoot, which is not to be used internally.”
Where it was sold
CO, GA, IA, KY physical locations. Nationwide via internet.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
84760

The 3 products recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-0707-2020 Class II

    Taspen's Organics Breathe Easy Herbal Tincture Dietary Supplement, sold in 1 oz, 2 oz, and 4 oz amber glass bottles with dropper.

    Codes: Lot numbers 1001 - 1254 Exp: 01/2020-10/2024

    Quantity: 197 units

  • F-0708-2020 Class II

    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.

    Codes: Lot numbers 1093 and 1108 Exp: 01/2020-10/2024

    Quantity: 268 units

  • F-0709-2020 Class II

    Taspen's Organics Respiratory Tea, sold in 2 oz packages

    Codes: Lot numbers 1001 - 1189 Exp: 01/2020-10/2024

    Quantity: 69 units

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of February 26, 2020.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.