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Basic Reset Inc.

Basic Reset Inc. Recalls

All product recalls associated with Basic Reset Inc..

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Recall Summary

Total Recalls

1000

Past Year

566

Class I (Serious)

25

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 3621–3640 of 7756 recalls

Q-min Supplement (Basic Reset) – Regulatory Non-Compliance (2019)

Products do not conform to Dietary Supplement CGMP regulations.

Class IIModerate

FDASep 23, 2019PR• Basic Reset Inc.

GH-C Supplement (Basic Reset) – Regulatory Non-Compliance (2019)

Products do not conform to Dietary Supplement CGMP regulations.

Class IIModerate

FDASep 23, 2019PR• Basic Reset Inc.

Body Mass Reset (Basic Reset Inc.) – CGMP Non-Compliance (2019)

Products do not conform to Dietary Supplement CGMP regulations.

Class IIModerate

FDASep 23, 2019PR• Basic Reset Inc.

SlimUp Capsules (Basic Reset Inc.) – CGMP Non-Compliance (2019)

Products do not conform to Dietary Supplement CGMP regulations.

Class IIModerate

FDASep 23, 2019PR• Basic Reset Inc.

pH-FX Supplement (Basic Reset) – Regulatory Non-Compliance (2019)

Products do not conform to Dietary Supplement CGMP regulations.

Class IIModerate

FDASep 23, 2019PR• Basic Reset Inc.

AquaLyte Supplement (Basic Reset) – Regulatory Non-Compliance (2019)

Products do not conform to Dietary Supplement CGMP regulations.

Class IIModerate

FDASep 23, 2019PR• Basic Reset Inc.

Mello-Tonin Supplement (Basic Reset) – Regulatory Non-Compliance (2019)

Products do not conform to Dietary Supplement CGMP regulations.

Class IIModerate

FDASep 23, 2019PR• Basic Reset Inc.

Dino Min Supplement (Basic Reset) – Regulatory Non-Compliance (2019)

Products do not conform to Dietary Supplement CGMP regulations.

Class IIModerate

FDASep 23, 2019PR• Basic Reset Inc.

Vibrant Energy Drink (Basic Reset Inc.) – CGMP Non-Compliance (2019)

Products do not conform to Dietary Supplement CGMP regulations.

Class IIModerate

FDASep 23, 2019PR• Basic Reset Inc.

Ionyte Supplement (Basic Reset) – Regulatory Non-Compliance (2019)

Products do not conform to Dietary Supplement CGMP regulations.

Class IIModerate

FDASep 23, 2019PR• Basic Reset Inc.

Beta Factor Supplement (Basic Reset) – Regulatory Non-Compliance (2019)

Products do not conform to Dietary Supplement CGMP regulations.

Class IIModerate

FDASep 23, 2019PR• Basic Reset Inc.

TRIM UP Dietary Supplement (Basic Reset Inc.) – CGMP Non-Compliance (2019)

Products do not conform to Dietary Supplement CGMP regulations.

Class IIModerate

FDASep 23, 2019PR• Basic Reset Inc.

Bee Gold Supplement (Basic Reset) – Regulatory Non-Compliance (2019)

Products do not conform to Dietary Supplement CGMP regulations.

Class IIModerate

FDASep 23, 2019PR• Basic Reset Inc.

Vibrant Energy Drink (Basic Reset) – Regulatory Non-Compliance (2019)

Products do not conform to Dietary Supplement CGMP regulations.

Class IIModerate

FDASep 23, 2019PR• Basic Reset Inc.

Baxter Healthcare Corporation: TherMax Blood Warmer Unit

TherMax Blood Warmers may not be in compliance with an electrical safety standard, which requires a protective earth connection that can sustain a current of 25 amps for 10 seconds.

FDASep 19, 2019Nationwide• Baxter Healthcare Corporation

Espinaler Razor Clams (A Priori Specialty Foods) – Foreign Object (2019)

An unknown object was found in a tin

Class IIModerate

FDASep 19, 2019AZ, CA, IA +8 more• YTM, Inc. DBA A Priori Specialty Foods

Baxter Healthcare Corporation: EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with...

Potential ability to leak once used for compounding.

FDASep 18, 2019Nationwide• Baxter Healthcare Corporation

Infant's Gas Relief Drops (GCP) – Microbial Contamination (2019)

Microbial Contamination of Non-Sterile Product.

Class IIModerate

FDASep 18, 2019Nationwide• GCP Laboratories Inc

Boston Scientific Corporation: iLab Polaris Multi-Modality Guidance System; ...

Certain iLab Polaris Systems which were upgraded with a previous 2.10 software version (disk batch 629774) contained a bug in which only the True Color Secondary Capture (SC) format will archive Diastolic Hyperemia-Free Ratio data as intended. If either Multi-Frame UltraSound (US) or SC Image Storage formats are used, the DFR data will not be archived and the user will not be notified of this unexpected behavior.

FDASep 18, 2019Nationwide• Boston Scientific Corporation

Lemon Dessert Bars (Schwartz Brothers) – undeclared egg (2019)

Lemon Dessert Bars product is recalled due to undeclared egg.

FDASep 16, 2019IN, WA• Schwartz Brothers Restaurants dba Schwartz Brothers Bakery

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