Green Water, LLC
FDA Regulatory Profile
Green Water, LLC has 10 FDA recalls, 4 inspections, 0 510(k) clearances and 1 compliance action on record.
- Latest recall
- F-0707-2020 · Class II · Oct 24, 2019
- Latest inspection
- Oct 5, 2026 · NAI
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Summary
Record counts and when each FDA source was last refreshed
| Records | Count | Last refreshed | Source as of | Status |
|---|
| Recalls | 10 | Nov 4, 2026 (checked Nov 8, 2026, unchanged) | File dated Nov 3, 2026 | Current |
|---|
| 510(k) clearances | 0 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
|---|
| Inspections | 4 | Nov 9, 2026 | Newest record Oct 28, 2026 | Current |
|---|
| Compliance actions | 1 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Recent Recalls
| Number | Class | Product | Date |
|---|
| F-0707-2020 | Class II | Taspen's Organics Breathe Easy Herbal Tincture Dietary Supplement, sold in 1 oz, 2 oz, and 4 oz… | Oct 24, 2019 |
| F-0708-2020 | Class II | Dragonfly Botanicals Full spectrum Breathe Deep 1000mg/oz Dietary Supplement, sold in 0.5 oz, 1 oz… | Oct 24, 2019 |
| F-0709-2020 | Class II | Taspen's Organics Respiratory Tea, sold in 2 oz packages | Oct 24, 2019 |
| F-2061-2019 | Class II | Taspen s Organics, Breathe Easy Herbal Tincture, Net wt 1 ounce, 2 ounce, 4 ounce | Jul 30, 2019 |
| F-2064-2019 | Class II | Taspen s Organics,Mojo Magic Herbal Tincture, Net wt 1 ounce, 2 ounce, 4 ounce | Jul 30, 2019 |
| F-2066-2019 | Class II | Taspens Organics, Organic Tea: Mothers Milk, 2 ounce. | Jul 30, 2019 |
| F-2060-2019 | Class II | Taspen s Organics, Bedroom Bliss Herbal Tincture, Net wt 1 ounce, 2 ounce, 4 ounce | Jul 30, 2019 |
| F-2063-2019 | Class II | Taspen s Organics,Happy Momma Herbal Tincture, Net wt 1 ounce, 2 ounce, 4 ounce | Jul 30, 2019 |
| F-2062-2019 | Class II | Taspen s Organics,Digest Ease Herbal Tincture, Net wt 1 ounce, 2 ounce, 4 ounce | Jul 30, 2019 |
| F-2065-2019 | Class II | Taspens Organics, Organic Tea: Respiratory, 2 ounce. | Jul 30, 2019 |
Recent FDA Inspections
NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|
| FEI 3010921677 | Conifer, CO | 4 | Oct 5, 2026 |