CLASS II Drug recall · Reported 13 Nov 2019 · FDA Enforcement Report
CBD Reset 2400, True Full Spectrum Natural (unflavored), 2400 mg CBD recalled
Basic Reset is recalling Basic Reset CBD Reset 2400, True Full Spectrum Natural (unflavored), 2400 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-0194-2020
- 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 2400, True Full Spectrum Natural (unflavored), 2400 mg CBD, 1 fl. oz. (29 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
Is CBD Reset 2400, True Full Spectrum Natural (unflavored), 2400 mg CBD recalled?
Yes. Basic Reset recalled CBD Reset 2400, True Full Spectrum Natural (unflavored), 2400 mg CBD on 18 Oct 2019. The recall is Class II and its status is Terminated. Recall number D-0194-2020.
Why was it recalled?
Marketed without an Approved NDA/ANDA
Which lots are affected?
Lot: 1903011.8
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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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