Food recall: OXZGEN Performance 25 mg Hemp Derived CBD + Teacrine + BCAA Orange Flavored, 5 blast caps, 2.2 FL OZ
Class II FDA enforcement event 83891. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Yellow #6 is not declared on ingredient label. The label lists Green Coffee Beans as an ingredient, but Guarana Seeds were used instead. The label lists the flavor as berry boost , but orange flavor was used.
Class II, in the words of FDA
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
Hall Global, LLC started this food recall on 25 Sep 2019. The firm address in the FDA record is in Southlake, TX. FDA put the recall in Class II. FDA event 83891 has 2 product records. The first FDA enforcement report date is 30 Oct 2019. The record gives the status Terminated, with the termination date 20 Feb 2020.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
Contract Manufacturer sends products to distribution centers owned by clients or direct to client company for distribution via internet to end product user.
Recalling firm
Hall Global, LLC, Southlake, TX.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
2 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-0070-2020 | OXZGEN Performance 25 mg Hemp Derived CBD + Teacrine + BCAA Orange Flavored, 5 blast caps, 2.2 FL OZ | 1007 packages of 5 count caps | Class II | Terminated | 30 Oct 2019 |
| F-0071-2020 | Sugar Mill Farms Focused Energy 25 mg Hemp Extract Berry Flavor 7.25 g 5 blast cap count | 4000 packages of 5 count blast caps | Class II | Terminated | 30 Oct 2019 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class II: The middle of the three FDA recall classes.
The event in context
- Food events that started in 2019
- 516
- Share of these events in Class II
- 56%
- Product records in this event
- 2
- Events of the firm on the register
- 1
Official channels
- FDA enforcement report F-0070-2020The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
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Cite this page
Recall Register. FDA enforcement event 83891. https://recallregister.com/fda/ii/83891/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
Contract Manufacturer sends products to distribution centers owned by clients or direct to client company for distribution via internet to end product user.
- What quantity of product is in FDA event 83891?
- The event has 2 product records. The first record gives this quantity:
1007 packages of 5 count caps
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2019 have the same class?
- 56% of the 516 food events that started in 2019 are in Class II.