CLASS II Food recall · Reported 27 Nov 2019 · FDA Enforcement Report

Beta Factor Dietary Supplement recalled by Basic Reset

Basic Reset is recalling Beta Factor Dietary Supplement per, distributed nationwide in the US. The recall was initiated on 23 Sep 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes1820705, 1806004, 1733404, 1815204, 1719204, W0002670, W0000304, W000325, W0003878

Quantity recalled262 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-0170-2020
FDA event ID: 83917
Recalling firm: Basic Reset, Hendersonville, TN
Brand: Beta Factor
Classification: Class II
Status: Terminated
Recall initiated: 23 Sep 2019
FDA classified: 21 Nov 2019
Reported: 27 Nov 2019
Type: FDA Mandated
Customers notified by: E-Mail
Reason category: Manufacturing (CGMP) Deviations
Product category: Dietary Supplements

Timeline

23 Sep 2019	Recall initiated by company
21 Nov 2019	Classified by FDA	+59 days
27 Nov 2019	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

Product as listed by the FDA

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

Where it was distributed

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.

Nationwide Puerto Rico

Questions about this recall

Why was it recalled?

Products do not conform to Dietary Supplement CGMP regulations.

Which lots are affected?

1820705, 1806004, 1733404, 1815204, 1719204, W0002670, W0000304, W000325, W0003878

Where was it sold?

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

13 other products · FDA event 83917

This product is part of a recall event; the main page for the event is Bee Gold pkg recalled by Basic Reset.

Reported	Class	Recall	Company	Reason	Where
27 Nov 2019	CLASS II	Bee Gold pkg recalled by Basic ResetBee Gold	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide
27 Nov 2019	CLASS II	Dino Min recalled by Basic ResetDino Min	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide
27 Nov 2019	CLASS II	Vibrant Energy Drink case) 100-4A and 100-4B recalled by Basic ResetVibrant	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide
27 Nov 2019	CLASS II	AquaLyte pkg recalled by Basic ResetAquaLyte	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide
27 Nov 2019	CLASS II	Trim UP Dietary Supplement recalled by Basic ResetTrim UP	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide
27 Nov 2019	CLASS II	pH-FX 4 fl. oz. plastic bottle, SKU: 100-1A recalled by Basic Reset	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide
27 Nov 2019	CLASS II	Ionyte 4 fl. oz. plastic bottle, SKU: 100-1B recalled by Basic ResetIonyte	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide
27 Nov 2019	CLASS II	Vibrant Energy Drink plastic canister 100-4A recalled by Basic ResetVibrant	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide
27 Nov 2019	CLASS II	Body Mass Reset recalled by Basic ResetBody Mass	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide
27 Nov 2019	CLASS II	Mello-Tonin 2 fl. oz. glass bottle, SKU: 100-5C recalled by Basic ResetMello-Tonin	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide
27 Nov 2019	CLASS II	Q-min recalled by Basic Reset	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide
27 Nov 2019	CLASS II	GH recalled by Basic Reset	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide
27 Nov 2019	CLASS II	SlimUp recalled by Basic ResetSlimUp	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide

More recalls from Basic Reset

All 26

Reported	Class	Recall	Company	Reason	Where
27 Nov 2019Food	CLASS II	SlimUp recalled by Basic ResetSlimUp	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide
27 Nov 2019Food	CLASS II	GH recalled by Basic Reset	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide
27 Nov 2019Food	CLASS II	Q-min recalled by Basic Reset	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide
27 Nov 2019Food	CLASS II	Mello-Tonin 2 fl. oz. glass bottle, SKU: 100-5C recalled by Basic ResetMello-Tonin	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide
27 Nov 2019Food	CLASS II	Body Mass Reset recalled by Basic ResetBody Mass	Basic Reset	Manufacturing (CGMP) Deviations	Nationwide

Other Dietary Supplements recalls

All 733

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21 Sep 2026Food	ANNOUNCED	Niwali Tejocote Capsules and Pieces recalled by Global MixNiwali	Global Mix	Foreign Material	Nationwide
2 Sep 2026Food	CLASS I	Addall XR Shot, liquid dietary supplement recalled by ZMB EnterprisesAddall XR	ZMB Enterprises	Hidden Drug Ingredients	CA
5 Aug 2026Food	CLASS II	Super Skin; Dietary Supplement;, 2 per day recalled by Mellish IslandMellish Island	Mellish Island	Other	Nationwide
29 Jul 2026Food	CLASS I	Modern Warrior Ready, Dietary Supplement recalledModern Warrior	Modern Warrior Life	Hidden Drug Ingredients	Nationwide
8 Jul 2026Food	CLASS II	Vista MAX; Dietary Supplement Serving Size recalled by Provision HealthVista MAX	Provision Health	Undeclared Allergens	CA