Hall Global Recalls OXZGEN CBD Capsules for Labeling Errors
Hall Global, LLC is recalling OXZGEN Performance CBD capsules because the label fails to declare Yellow #6 and lists an incorrect amount of Vitamin B2.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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 involves minor labeling errors regarding an undeclared color additive and incorrect vitamin dosage, which fits the rubric for moderate severity.
Plain-English summary
Hall Global, LLC is recalling OXZGEN Performance 25 mg Hemp Derived CBD + Teacrine + BCAA Orange Flavored, 5 blast caps, 2.2 FL OZ. The recall involves 1,007 packages of 5 count caps. The product was distributed to distribution centers owned by clients or directly to client companies for distribution via the internet to end product users.
The recall was initiated due to labeling inaccuracies. Specifically, Yellow #6 is not declared on the ingredient label, and the label claim for Vitamin B2 (B2) is incorrect, stating 10 mg when the product actually contains 5 mg.
Consumers with this product should stop using it and contact the recalling firm for instructions on return or disposal. The affected lot codes are 10097902, 10186904, 10235905, and 10278906.
The recalled product
- Product
- OXZGEN Performance 25 mg Hemp Derived CBD + Teacrine + BCAA Orange Flavored, 5 blast caps, 2.2 FL OZ
- Manufacturer
- Hall Global, LLC
- Category
- Food — Dietary Supplement
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 (4)
- 10097902
- 10186904
- 10235905
- and 10278906
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 2 recalled by Hall Global, LLC 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 2 products in this recall →Related recalls
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