D-0190-2020 Class II Terminated

Recalled by Basic Reset Inc. — Hendersonville, TN

FDA drug recall D-0190-2020 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: 339 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
339 bottles

Product Description

Nuovi Firming Masque, Renew and Reset, 2 fl. oz. 59 mL bottle, Made in USA exclusively for Basic Reset 260 W. Main St., Ste 103 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: 30995

Source

Dataset
openFDA drug recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for D-0190-2020
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-0190-2020. Report a data issue: hello@regdatalab.com.