CLASS II Food recall · Reported 27 Nov 2019 · FDA Enforcement Report
Vibrant Energy Drink plastic canister 100-4A recalled by Basic Reset
Basic Reset is recalling Vibrant Energy Drink plastic canister 100-4A, distributed nationwide in the US. The recall was initiated on 23 Sep 2019 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-0172-2020
- FDA event ID
- 83917
- Recalling firm
- Basic Reset, Hendersonville, TN
- Brand
- Vibrant
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 23 Sep 2019
- FDA classified
- 21 Nov 2019
- Reported
- 27 Nov 2019
- Type
- FDA Mandated
- Customers notified by
- Reason category
- Manufacturing (CGMP) Deviations
- Product category
- Energy Drinks
Timeline
| 23 Sep 2019 | Recall initiated by company | |
| 21 Nov 2019 | Classified by FDA | +59 days |
| 27 Nov 2019 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Products do not conform to Dietary Supplement CGMP regulations.
Product as listed by the FDA
Vibrant ENERGY DRINK 450 g plastic canister 100-4A
Where it was distributed
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.
Questions about this recall
Why was it recalled?
Products do not conform to Dietary Supplement CGMP regulations.
Which lots are affected?
01190P06576
Where was it sold?
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.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
13 other products · FDA event 83917This product is part of a recall event; the main page for the event is Bee Gold pkg recalled by Basic Reset.
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