Recall · openFDA Food Enforcement

BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle…: FDA Recall F-0170-2020

Agency action: Sep 23, 2019Record ID: F-0170-2020
View official source ↗

What happened

Original notice title

BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F, recall F-0170-2020

From the archived source record

Products do not conform to Dietary Supplement CGMP regulations.

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

Read the official notice →

Status and source details

Status recorded in the archive
Terminated
FDA recall classification
Class II
Recall initiated by
FDA Mandated
Report date
Nov 27, 2019
Termination date in the archive
Aug 19, 2020
Source checked
Jul 16, 2026
Record revision
d235097053f7

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

Sources, dates, and coverage →

What is affected

Product
BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F
Company
Basic Reset Inc.
Lot / identifier
1820705, 1806004, 1733404, 1815204, 1719204, W0002670, W0000304, W000325, W0003878
Market / distribution
Product was shipped to all 50 states. Product was shipped to the following foreign consignees: Canada, Nigeria, U.K., Australia, Israel, Puerto Rico, Virgin Islands, Hungary, UAE, Mexico, Philippines, Greece, and Puerto Rico.