Basic Reset CBD Reset 750 True Full Spectrum Natural Flavor 750 mg… — Class II drug recall D-0193-2020
Terminated recall by Basic Reset Inc., reported 2019-11-13, distributed in PR, VI. Marketed without an Approved NDA/ANDA
| Recall number | D-0193-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA mandated |
| Recalling firm | Basic Reset Inc., Hendersonville, TN, United States |
| Recall initiated | 2019-10-18 |
| Classified | 2019-11-05 |
| Reported by FDA | 2019-11-13 |
| Terminated | 2021-10-27 |
| Distributed | PR, VI |
| Countries outside the US | AE, AU, CA, GB, GR, HU, IL, MX, NG, PH |
| Quantity | 98 bottles |
| Reason classes | unapproved product |
| Lot numbers | 1916911.25 |
Product
Basic Reset CBD Reset 750 True Full Spectrum Natural Flavor 750 mg CBD 1 fl. oz. (30 mL) bottle, Distributed by: Basic Reset Hendersonville, TN 37075
Reason for recall
Marketed without an Approved NDA/ANDA
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0193-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.