Basic Reset Inc. FDA recall records

The FDA has published 14 food recall enforcement records naming Basic Reset Inc. between 2019 and 2019, covering 1 separate recall events. The firm is recorded in Tennessee. Data last updated 2 September 2026.

Records of 29,386
14
Share of all recalls
0%
Class I of 14
0
Reported between
2019 to 2019

What these records are

Every record on this page was published by the FDA in the openFDA food enforcement database. 14 records cover 1 recall events, because the agency opens one record per product code: a single recall of a product line with many codes appears here many times.

0 of these records are Class I, 14 Class II and 0 Class III. A recall count is not a safety score. Most FDA food recalls are initiated by the firm itself, and a recall is the firm removing product from the market, which is what a food safety plan is built to produce.

By year

Counts are by the date the FDA reported the enforcement action. That date runs behind the date a firm started a recall, so the most recent year is always partial.

Where the recalling firms are

The state is the location of the recalling firm, not where the product was sold. Distribution is recorded separately on each record.

Most recently reported

All 14 records.
ReportedProductFirmReasonClass
2019-11-27Bee Gold 8oz. pkg./plastic pouch, SKU: 100-4CBasic Reset Inc.Products do not conform to Dietary Supplement CGMP regulations.Class II
2019-11-27Dino Min, 60 capsules per plastic bottle, SKU: 100-1CBasic Reset Inc.Products do not conform to Dietary Supplement CGMP regulations.Class II
2019-11-27Vibrant ENERGY DRINK 15 g foil pouches (15 pack case) 100-4A and 100-4BBasic Reset Inc.Products do not conform to Dietary Supplement CGMP regulations.Class II
2019-11-27AquaLyte, 30g pkg./foil pouch, SKU: 1023Basic Reset Inc.Products do not conform to Dietary Supplement CGMP regulations.Class II
2019-11-27TRIM UP DIETARY SUPPLEMENT 80 capsules per plastic bottle, SKU: 100-5ABasic Reset Inc.Products do not conform to Dietary Supplement CGMP regulations.Class II
2019-11-27pH-FX 4 fl. oz. plastic bottle, SKU: 100-1ABasic Reset Inc.Products do not conform to Dietary Supplement CGMP regulations.Class II
2019-11-27Ionyte 4 fl. oz. plastic bottle, SKU: 100-1BBasic Reset Inc.Products do not conform to Dietary Supplement CGMP regulations.Class II
2019-11-27Vibrant ENERGY DRINK 450 g plastic canister 100-4ABasic Reset Inc.Products do not conform to Dietary Supplement CGMP regulations.Class II
2019-11-27Body Mass Reset, 4 fl. oz. plastic bottle, SKU: 100-8CBasic Reset Inc.Products do not conform to Dietary Supplement CGMP regulations.Class II
2019-11-27Mello-Tonin 2 fl. oz. glass bottle, SKU: 100-5CBasic Reset Inc.Products do not conform to Dietary Supplement CGMP regulations.Class II
2019-11-27Q-min, 50 capsules per plastic bottle, SKU: 100-9BBasic Reset Inc.Products do not conform to Dietary Supplement CGMP regulations.Class II
2019-11-27BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4FBasic Reset Inc.Products do not conform to Dietary Supplement CGMP regulations.Class II
2019-11-27GH-C, 60 capsules per plastic bottle, SKU: 100-4FBasic Reset Inc.Products do not conform to Dietary Supplement CGMP regulations.Class II
2019-11-27SlimUp 60 capsules per plastic bottle, SKU: 100-5BBasic Reset Inc.Products do not conform to Dietary Supplement CGMP regulations.Class II

Questions

How many FDA recalls has Basic Reset Inc. had?
The FDA has published 14 food recall enforcement records naming Basic Reset Inc. between 2019 and 2019. Those records cover 1 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.
Does a high recall count mean a firm is unsafe?
Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.

All FDA food recall data

A recall is the end of an evidence trail that either existed or did not. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.