CLASS II Drug recall · Reported 13 Nov 2019 · FDA Enforcement Report
CBD Reset 750 True Full Spectrum Wintergreen, 750 mg CBD recalled
Basic Reset is recalling CBD Reset 750 True Full Spectrum Wintergreen, 750 mg CBD, distributed in Puerto Rico. The recall was initiated on 18 Oct 2019 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0191-2020
- FDA event ID
- 83997
- Recalling firm
- Basic Reset, Hendersonville, TN
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 18 Oct 2019
- FDA classified
- 5 Nov 2019
- Reported
- 13 Nov 2019
- Type
- FDA Mandated
- Customers notified by
- Letter
- Reason category
- Other Reasons
Timeline
| 18 Oct 2019 | Recall initiated by company | |
| 5 Nov 2019 | Classified by FDA | +18 days |
| 13 Nov 2019 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Marketed without an Approved NDA/ANDA
Product as listed by the FDA
Basic Reset CBD Reset 750 True Full Spectrum Wintergreen, 750 mg CBD, 1 fl. oz. (30 mL) bottle, Distributed by: Basic Reset Hendersonville, TN 37075
Where it was distributed
United States including Puerto Rico and U.S. Virgin Islands, Canada, Nigeria, United Kingdom, Australia, Israel, Hungary, UAE, Mexico, Philippines, Greece
Questions about this recall
Why was it recalled?
Marketed without an Approved NDA/ANDA
Which lots are affected?
Lots: 1902411.25, 1916911.25
Where was it sold?
United States including Puerto Rico and U.S. Virgin Islands, Canada, Nigeria, United Kingdom, Australia, Israel, Hungary, UAE, Mexico, Philippines, Greece
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
10 other products · FDA event 83997This product is part of a recall event; the main page for the event is Miracle Facelift Masque, All Natural, The Miracle recalled.
More recalls from Basic Reset
All 26| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Food | CLASS II | SlimUp recalled by Basic ResetSlimUp | Basic Reset | Manufacturing (CGMP) Deviations | Nationwide |
| Food | CLASS II | GH recalled by Basic Reset | Basic Reset | Manufacturing (CGMP) Deviations | Nationwide |
| Food | CLASS II | Beta Factor Dietary Supplement recalled by Basic ResetBeta Factor | Basic Reset | Manufacturing (CGMP) Deviations | Nationwide |
| Food | CLASS II | Q-min recalled by Basic Reset | Basic Reset | Manufacturing (CGMP) Deviations | Nationwide |
| Food | CLASS II | Mello-Tonin 2 fl. oz. glass bottle, SKU: 100-5C recalled by Basic ResetMello-Tonin | Basic Reset | Manufacturing (CGMP) Deviations | Nationwide |