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

Lot, batch or date codes01190P06576
Quantity recalled1980 canisters

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
E-Mail
Reason category
Foreign Material
Product category
Energy Drinks

Timeline

23 Sep 2019Recall initiated by company
21 Nov 2019Classified by FDA+59 days
27 Nov 2019Published 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.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

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.

Nationwide Puerto Rico

Questions about this recall

Is Vibrant Energy Drink plastic canister 100-4A recalled?

Yes. Basic Reset recalled Vibrant Energy Drink plastic canister 100-4A on 23 Sep 2019. The recall is Class II and its status is Terminated. Recall number F-0172-2020.

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 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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