D-0194-2020 Class II Terminated

Recalled by Basic Reset Inc. — Hendersonville, TN

FDA drug recall D-0194-2020 was initiated by Basic Reset Inc. on Oct 18, 2019 and is designated Class II. Reason for recall: Marketed without an Approved NDA/ANDA The recall status is terminated (terminated Oct 27, 2021). Affected quantity: 391 bottles.

Recall Details

Product Type
Drugs
Report Date
Nov 13, 2019
Initiation Date
Oct 18, 2019
Termination Date
Oct 27, 2021
Voluntary/Mandated
FDA Mandated
Product Quantity
391 bottles

Product Description

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

Reason for Recall

Marketed without an Approved NDA/ANDA

Distribution Pattern

United States including Puerto Rico and U.S. Virgin Islands, Canada, Nigeria, United Kingdom, Australia, Israel, Hungary, UAE, Mexico, Philippines, Greece

Code Information

Lot: 1903011.8

Source

Dataset
openFDA drug recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for D-0194-2020
openFDA file date
Nov 3, 2026
Loaded by RegDataLab
Nov 4, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for D-0194-2020. Report a data issue: hello@regdatalab.com.