Basic Reset Bee Gold 8oz recall — FDA F-0174-2020
Products do not conform to Dietary Supplement CGMP regulations.
Overview of recall records associated with Basic Reset Inc., including dates, categories and classifications where available.
Classification mix: Class II: 26.
Products do not conform to Dietary Supplement CGMP regulations.
Products do not conform to Dietary Supplement CGMP regulations.
Products do not conform to Dietary Supplement CGMP regulations.
Products do not conform to Dietary Supplement CGMP regulations.
Products do not conform to Dietary Supplement CGMP regulations.
Products do not conform to Dietary Supplement CGMP regulations.
Products do not conform to Dietary Supplement CGMP regulations.
Products do not conform to Dietary Supplement CGMP regulations.
Products do not conform to Dietary Supplement CGMP regulations.
Products do not conform to Dietary Supplement CGMP regulations.
Products do not conform to Dietary Supplement CGMP regulations.
Products do not conform to Dietary Supplement CGMP regulations.
Products do not conform to Dietary Supplement CGMP regulations.
Products do not conform to Dietary Supplement CGMP regulations.
FDA determined that marketing claims surrounding product rendered product a medical device which was adulterated and misbranded.
Marketed without an Approved NDA/ANDA
Marketed without an Approved NDA/ANDA
Marketed without an Approved NDA/ANDA
Marketed without an Approved NDA/ANDA
Marketed without an Approved NDA/ANDA
Marketed without an Approved NDA/ANDA
Marketed without an Approved NDA/ANDA
Marketed without an Approved NDA/ANDA
Marketed without an Approved NDA/ANDA
This page summarizes recall records in which the official source identifies Basic Reset Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.