Basic Reset Recalls Bee Gold Dietary Supplements for CGMP Violations
Basic Reset Inc. is recalling Bee Gold dietary supplements because they do not conform to Dietary Supplement CGMP regulations.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the source text cites non-conformance to CGMP regulations without reporting specific illnesses, injuries, or high-risk pathogens, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
Basic Reset Inc. is voluntarily recalling Bee Gold 8oz. pkg./plastic pouch (SKU: 100-4C) because the products do not conform to Dietary Supplement Current Good Manufacturing Practice (CGMP) regulations. The recall is classified as FDA Class II.
The affected product was shipped to all 50 states and to foreign consignees in Canada, Nigeria, the U.K., Australia, Israel, Puerto Rico, the Virgin Islands, Hungary, UAE, Mexico, the Philippines, and Greece. Specific lot codes associated with the recall include ZCBEEPF1881, 2018061, 2018105, ZCBEEPG2935, and ZCBEEPG3724.
Consumers who have purchased this product should check their lot codes against the list provided by the FDA and stop using the product if it matches. For more information, consumers should contact the recalling firm or refer to the FDA recall notice.
The recalled product
- Product
- Bee Gold 8oz. pkg./plastic pouch, SKU: 100-4C
- Manufacturer
- Basic Reset Inc.
- Category
- Food — Dietary Supplements
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (5)
- ZCBEEPF1881
- 2018061
- 2018105
- ZCBEEPG2935
- ZCBEEPG3724
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 14 recalled by Basic Reset Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 14 products in this recall →Related recalls
Same manufacturer · Basic Reset Inc.
See all →- ModerateBasic Reset Dino Min Dietary Supplement Recalled for CGMP Non-Compliance
FDA (Food) · 2019-11-27
- ModerateBasic Reset Recalls Trim Up Dietary Supplement for CGMP Violations
FDA (Food) · 2019-11-27
- ModerateBasic Reset Recalls Beta Factor Dietary Supplement for CGMP Violations
FDA (Food) · 2019-11-27
- ModerateBasic Reset Recalls AquaLyte Dietary Supplement for CGMP Violations
FDA (Food) · 2019-11-27
- ModerateBasic Reset Recalls Vibrant Energy Drink for CGMP Violations
FDA (Food) · 2019-11-27
Same hazard · cgmp violation
See all →- Moderatevite20 Antifungal Cream recalled due to stability testing deviations
FDA (Drugs) · 2026-07-08
- ModerateNeuroquell products recalled over current good manufacturing practice violations
FDA (Drugs) · 2025-09-17
- ModerateOptim V Anti-Itch Cream Recalled for Current Good Manufacturing Practice Deviations
FDA (Drugs) · 2025-05-28
- ModerateNature Mint Anticavity Fluoride Toothpaste Recalled for CGMP Deviations
FDA (Drugs) · 2025-05-28
- ModerateRapidol Hydrocortisone 1% Anti-Itch Cream Recalled for CGMP Deviations
FDA (Drugs) · 2025-05-28