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FDA recall record

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.

Recall F-0708-2020Class IITerminatedOctober 24, 2019

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of June 7, 2021. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

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.

Reason

The products contain Coltsfoot, which is not to be used internally.

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

  • 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.

Code information listed by FDA

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

Distribution and firm information

Recalling firm listed by FDA: Green Water, LLC

Firm location listed by FDA: Conifer, CO, United States

Distribution reported by FDA: CO, GA, IA, KY physical locations. Nationwide via internet.

Product quantity listed by FDA: 268 units

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.