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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food
Food & Beverages/Dietary Supplements

Basic Reset Dietary Supplements Recalled for Quality Regulation Violations

Agency Publication Date: November 21, 2019
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Summary

Basic Reset Inc. is recalling approximately 11,594 units of various dietary supplements and energy drinks because they do not conform to Current Good Manufacturing Practice (CGMP) regulations. These products include items like BETA FACTOR, TRIM UP, and Vibrant ENERGY DRINK, which were distributed across all 50 U.S. states and several international countries. Because the products were not manufactured according to required safety and quality standards, the company cannot guarantee their identity, purity, strength, or composition. Consumers should return these products to the place of purchase for a refund or throw them away.

Risk

Failure to follow Good Manufacturing Practices means these supplements may contain incorrect ingredients or levels of potency, posing a moderate risk to health as the safety and quality of the products cannot be verified.

What You Should Do

  1. Identify if you have any of the affected Basic Reset products by checking the product name and SKU on the bottle or canister. Affected items include BETA FACTOR (SKU 100-4F), TRIM UP (SKU 100-5A), Vibrant ENERGY DRINK (SKU 100-4A/B), Bee Gold (SKU 100-4C), Ionyte (SKU 100-1B), Mello-Tonin (SKU 100-5C), pH-FX (SKU 100-1A), SlimUp (SKU 100-5B), AquaLyte (SKU 1023), Body Mass Reset (SKU 100-8C), GH-C (SKU 100-4F), Q-min (SKU 100-9B), and Dino Min (SKU 100-1C).
  2. Check the lot numbers or batch codes printed on your product packaging. See the Affected Products section below for the full list of affected codes.
  3. Return the product to the place of purchase for a full refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: BETA FACTOR DIETARY SUPPLEMENT (60 capsules)
Item Code:
100-4F
Lot Numbers:
1820705
1806004
1733404
1815204
1719204
W0002670
W0000304
W000325
W0003878

Recall #: F-0170-2020

Product: TRIM UP DIETARY SUPPLEMENT (80 capsules)
Item Code:
100-5A
Lot Numbers:
ACRXI
ADMUA

Recall #: F-0171-2020

Product: Vibrant ENERGY DRINK (450 g plastic canister)
Item Code:
100-4A
Lot Numbers:
01190P06576

Recall #: F-0172-2020

Product: Vibrant ENERGY DRINK (15 g foil pouches, 15 pack case)
Item Code:
100-4A
100-4B
Lot Numbers:
F1246L
P12317

Recall #: F-0173-2020

Product: Bee Gold (8oz. pkg./plastic pouch)
Item Code:
100-4C
Lot Numbers:
ZCBEEPF1881
2018061
2018105
ZCBEEPG2935
ZCBEEPG3724

Recall #: F-0174-2020

Product: Ionyte (4 fl. oz. plastic bottle)
Item Code:
100-1B
Lot Numbers:
29049
28343
27618A
19018B
35317B
101617
08518A
29123

Recall #: F-0175-2020

Product: Mello-Tonin (2 fl. oz. glass bottle)
Item Code:
100-5C
Lot Numbers:
180209-BSC2354
170801-BSC2354

Recall #: F-0176-2020

Product: pH-FX (4 fl. oz. plastic bottle)
Item Code:
100-1A
Lot Numbers:
29031
28231
28335
28175
28057
80324
29119

Recall #: F-0177-2020

Product: SlimUp (60 capsules per plastic bottle)
Item Code:
100-5B
Lot Numbers:
170801-BSC2130

Recall #: F-0178-2020

Product: AquaLyte (30g pkg./foil pouch)
Item Code:
1023
Lot Numbers:
91117

Recall #: F-0179-2020

Product: Body Mass Reset (4 fl. oz. plastic bottle)
Item Code:
100-8C
Lot Numbers:
40517

Recall #: F-0180-2020

Product: GH-C (60 capsules per plastic bottle)
Item Code:
100-4F
Lot Numbers:
71917
GH7-17

Recall #: F-0181-2020

Product: Q-min (50 capsules per plastic bottle)
Item Code:
100-9B
Lot Numbers:
170801-BSC0462

Recall #: F-0182-2020

Product: Dino Min (60 capsules per plastic bottle)
Item Code:
100-1C
Lot Numbers:
02219A
27418A
22618B
18919A
11618B
07819A
06118D
36017B

Recall #: F-1239-2020

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 83917
Status: Resolved
Manufacturer: Basic Reset Inc.
Sold By: Basic Reset Inc.
Manufactured In: United States
Units Affected: 4 products (262 bottles; 2465 bottles; 1980 canisters; 6887 cases)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.