Basic Reset Inc.

Complete recall history across all FDA and CPSC categories — 26 total recalls

Basic Reset Inc. appears in recall records across 3 categories. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Food Recalls (14)

FDA food safety enforcement actions by Basic Reset Inc.

Date Product Reason Class
Sep 23, 2019 SlimUp 60 capsules per plastic bottle, SKU: 100-5B Products do not conform to Dietary Supplement CGMP regulations. Class II
Sep 23, 2019 GH-C, 60 capsules per plastic bottle, SKU: 100-4F Products do not conform to Dietary Supplement CGMP regulations. Class II
Sep 23, 2019 BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F Products do not conform to Dietary Supplement CGMP regulations. Class II
Sep 23, 2019 Q-min, 50 capsules per plastic bottle, SKU: 100-9B Products do not conform to Dietary Supplement CGMP regulations. Class II
Sep 23, 2019 Mello-Tonin 2 fl. oz. glass bottle, SKU: 100-5C Products do not conform to Dietary Supplement CGMP regulations. Class II
Sep 23, 2019 Body Mass Reset, 4 fl. oz. plastic bottle, SKU: 100-8C Products do not conform to Dietary Supplement CGMP regulations. Class II
Sep 23, 2019 Vibrant ENERGY DRINK 450 g plastic canister 100-4A Products do not conform to Dietary Supplement CGMP regulations. Class II
Sep 23, 2019 Ionyte 4 fl. oz. plastic bottle, SKU: 100-1B Products do not conform to Dietary Supplement CGMP regulations. Class II
Sep 23, 2019 pH-FX 4 fl. oz. plastic bottle, SKU: 100-1A Products do not conform to Dietary Supplement CGMP regulations. Class II
Sep 23, 2019 TRIM UP DIETARY SUPPLEMENT 80 capsules per plastic bottle, SKU: 100-5A Products do not conform to Dietary Supplement CGMP regulations. Class II
Sep 23, 2019 AquaLyte, 30g pkg./foil pouch, SKU: 1023 Products do not conform to Dietary Supplement CGMP regulations. Class II
Sep 23, 2019 Vibrant ENERGY DRINK 15 g foil pouches (15 pack case) 100-4A and 100-4B Products do not conform to Dietary Supplement CGMP regulations. Class II
Sep 23, 2019 Dino Min, 60 capsules per plastic bottle, SKU: 100-1C Products do not conform to Dietary Supplement CGMP regulations. Class II
Sep 23, 2019 Bee Gold 8oz. pkg./plastic pouch, SKU: 100-4C Products do not conform to Dietary Supplement CGMP regulations. Class II

Drug Recalls (11)

FDA drug safety enforcement actions by Basic Reset Inc.

Date Product Reason Class
Oct 18, 2019 Basic Reset CBD Reset 2400, True Full Spectrum Natural (unflavored), 2400 mg ... Marketed without an Approved NDA/ANDA Class II
Oct 18, 2019 BIOGENYX True Full Spectrum CBD Oil Cinnamon, 1 fl. oz. (30 mL) bottle, 750 m... Marketed without an Approved NDA/ANDA Class II
Oct 18, 2019 BIOGENYX True Full Spectrum CBD Oil Wintergreen, 1 fl. oz. (30 mL) bottle, 75... Marketed without an Approved NDA/ANDA Class II
Oct 18, 2019 Nuovi Firming Masque, Renew and Reset, 2 fl. oz. 59 mL bottle, Made in USA ex... Marketed without an Approved NDA/ANDA Class II
Oct 18, 2019 BIOGENYX True Full Spectrum CBD Oil Natural Flavor, 1 fl. oz. (30 mL) bottle,... Marketed without an Approved NDA/ANDA Class II
Oct 18, 2019 Basic Reset CBD Reset 750 True Full Spectrum Wintergreen, 750 mg CBD, 1 fl. o... Marketed without an Approved NDA/ANDA Class II
Oct 18, 2019 Basic Reset CBD Reset 750 True Full Spectrum Natural Flavor 750 mg CBD 1 fl. ... Marketed without an Approved NDA/ANDA Class II
Oct 18, 2019 Basic Reset Earth Wash Cleaner and Personal Care, Eco Friendly, Non Toxic, 2 ... Marketed without an Approved NDA/ANDA Class II
Oct 18, 2019 Basic Reset Nuovi Skin Toner, Refined Ionyte, 4 FL. OZ., 118.3 mL bottle, Dis... Marketed without an Approved NDA/ANDA Class II
Oct 18, 2019 Basic Reset CBD Reset 750 True Full Spectrum Cinnamon, 750 mg CBD, 1 fl. oz. ... Marketed without an Approved NDA/ANDA Class II
Oct 18, 2019 Miracle Facelift Masque, All Natural, The Miracle in a Bottle, 2 fl. oz./60 m... Marketed without an Approved NDA/ANDA Class II

Device Recalls (1)

FDA medical device enforcement actions by Basic Reset Inc.

Date Product Reason Class
Oct 18, 2019 Energy FX: a) original Aluminum (100-3A) b) sleek (adult and kid & pet) (1... FDA determined that marketing claims surrounding product rendered product a m... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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