17%

Fewer recalls than
Beverages peers

Basic Reset — FDA Recall History & Enforcement Records

Established Player · Beverages

Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.

As of July 16, 2026, Basic Reset has 14 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 23 Sep 2019. Basic Reset is categorized under Beverages based on their predominant recall history.

14
Total FDA recalls
6.8
Years in FDA database
2.1
Recalls per year
2,488 days(6.8 yrs)
Since last recall
0.0%
Class I (life-threatening)
2.1 recalls/yr vs Beverages avg 1.5/yrWell Above Average

Recall activity over time for Basic Reset

How serious are Basic Reset recalls?

FDA recall classifications by severity

Class I (Life-threatening)
0.0% (0 recalls)
Class II (Moderate risk)
100.0% (14 recalls)
Class III (Minor violation)
0.0% (0 recalls)

Full FDA recall history for Basic Reset

All 14 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first

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

Where have Basic Reset recalls occurred?

States affected across all recorded FDA enforcement actions

See individual recall notices

Where does this recall data come from?

Verification required: FoodRecallFinder.com cannot verify the safety of individual food products in your possession. Always verify the current recall status at FDA.gov before disposing of or consuming a product.

Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.

To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.

© 2026 FoodRecallFinder.com | Turnkey Trading Unlimited LLC. All rights reserved. FDA recall data sourced from openFDA.gov.

How we calculate these metrics →