Basic Reset Bee Gold 8oz Pouches: Dietary Supplement CGMP Non-Compliance
Basic Reset recalls Bee Gold 8oz plastic pouches due to failure to meet dietary supplement manufacturing regulations. Consumers should check product codes for affected items.
Lower-risk recall
Products do not conform to Dietary Supplement CGMP regulations.
Contact the company
What happened, in plain English
Basic Reset is recalling Bee Gold 8oz plastic pouches because they don't meet dietary supplement manufacturing regulations. This means the product may not be safe or properly labeled as required by law. Read more at govinfonow.com/recall/16610-basic-reset-bee-gold-8oz-pouches-dietary-supplement-cgmp-non.
Source Summary by GovInfoNow · govinfonow.com/recall/16610-basic-reset-bee-gold-8oz-pouches-dietary-supplement-cgmp-non · Updated October 5, 2026 · FDA enforcement record: FDA #F-0174-2020
Cite this page
“Basic Reset Bee Gold 8oz Pouches: Dietary Supplement CGMP Non-Compliance.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16610-basic-reset-bee-gold-8oz-pouches-dietary-supplement-cgmp-non. Based on FDA recall #F-0174-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0174-2020%22&limit=1).
Why it’s dangerous
The product fails to meet dietary supplement manufacturing regulations, which means it may not be safe or properly labeled. This could lead to incorrect supplement information or potential safety issues.
Who’s affected
People who bought Bee Gold 8oz pouches from stores or online. Those most at risk are consumers who use the product for dietary supplements.
How to tell if you have this one
Check for the SKU codes: 100-4C, ZCBEEPF1881, 2018061, 2018105, ZCBEEPG2935, ZCBEEPG3724. The product is sold in 8oz plastic pouches.
- Brand
Basic Reset- Category
Food
All 14 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
Product was shipped to all 50 states. Product was shipped to the following foreign consignees: Canada, Nigeria, U.K., Australia, Israel, Puerto Rico, Virgin Islands, Hungary, UAE, Mexico, Philippines, Greece, and Puerto Rico.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-0170-2020 | BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F; 1820705, 1806004, 1733404, 1815204, 1719204, W0002670, W0000304, W000325, W0003878 | 262 bottles |
| F-0171-2020 | TRIM UP DIETARY SUPPLEMENT 80 capsules per plastic bottle, SKU: 100-5A; ACRXI, ADMUA | 2465 bottles |
| F-0172-2020 | Vibrant ENERGY DRINK 450 g plastic canister 100-4A; 01190P06576 | 1980 canisters |
| F-0173-2020 | Vibrant ENERGY DRINK 15 g foil pouches (15 pack case) 100-4A and 100-4B; F1246L and P12317 | 6887 cases |
| F-0174-2020 | Bee Gold 8oz. pkg./plastic pouch, SKU: 100-4C; ZCBEEPF1881, 2018061, 2018105, ZCBEEPG2935, ZCBEEPG3724 | N/A |
| F-0175-2020 | Ionyte 4 fl. oz. plastic bottle, SKU: 100-1B; 29049,28343,27618A,19018B, 35317B,101617,08518A, 29123 | N/A |
| F-0176-2020 | Mello-Tonin 2 fl. oz. glass bottle, SKU: 100-5C; 180209-BSC2354, 170801-BSC2354 | N/A |
| F-0177-2020 | pH-FX 4 fl. oz. plastic bottle, SKU: 100-1A; 29031,28231,28335,28175, 28057, 80324, 29119 | N/A |
| F-0178-2020 | SlimUp 60 capsules per plastic bottle, SKU: 100-5B; 170801-BSC2130 | N/A |
| F-0179-2020 | AquaLyte, 30g pkg./foil pouch, SKU: 1023; 91117 | N/A |
| F-0180-2020 | Body Mass Reset, 4 fl. oz. plastic bottle, SKU: 100-8C; 40517 | N/A |
| F-0181-2020 | GH-C, 60 capsules per plastic bottle, SKU: 100-4F; 71917, GH7-17 | N/A |
| F-0182-2020 | Q-min, 50 capsules per plastic bottle, SKU: 100-9B; 170801-BSC0462 | N/A |
| F-1239-2020 | Dino Min, 60 capsules per plastic bottle, SKU: 100-1C; 02219A, 27418A, 22618B, 18919A, 11618B, 07819A, 06118D, 36017B | N/A |
What to do — step by step
Check Product Codes
Look for the SKU codes listed: 100-4C, ZCBEEPF1881, 2018061, 2018105, ZCBEEPG2935, ZCBEEPG3724.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
FDA distribution: “Product was shipped to all 50 states. Product was shipped to the following foreign consignees: Canada, Nigeria, U.K., Australia, Israel, Puerto Rico, Virgin Islands, Hungary, UAE, Mexico, Philippines, Greece, and Puerto Rico.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 11 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0174-2020 (September 23, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0174-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.