Food recall: BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F
Class II FDA enforcement event 83917. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Products do not conform to Dietary Supplement CGMP regulations.
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
Basic Reset Inc. started this food recall on 23 Sep 2019. The firm address in the FDA record is in Hendersonville, TN. FDA put the recall in Class II. FDA event 83917 has 14 product records. The first FDA enforcement report date is 27 Nov 2019. The record gives the status Terminated, with the termination date 19 Aug 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.
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,…
Recalling firm
Basic Reset Inc., Hendersonville, TN.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: FDA Mandated.
Products
14 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-0170-2020 | BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F | 262 bottles | Class II | Terminated | 27 Nov 2019 |
| F-0171-2020 | TRIM UP DIETARY SUPPLEMENT 80 capsules per plastic bottle, SKU: 100-5A | 2465 bottles | Class II | Terminated | 27 Nov 2019 |
| F-0172-2020 | Vibrant ENERGY DRINK 450 g plastic canister 100-4A | 1980 canisters | Class II | Terminated | 27 Nov 2019 |
| F-0173-2020 | Vibrant ENERGY DRINK 15 g foil pouches (15 pack case) 100-4A and 100-4B | 6887 cases | Class II | Terminated | 27 Nov 2019 |
| F-0174-2020 | Bee Gold 8oz. pkg./plastic pouch, SKU: 100-4C | N/A | Class II | Terminated | 27 Nov 2019 |
| F-0175-2020 | Ionyte 4 fl. oz. plastic bottle, SKU: 100-1B | N/A | Class II | Terminated | 27 Nov 2019 |
| F-0176-2020 | Mello-Tonin 2 fl. oz. glass bottle, SKU: 100-5C | N/A | Class II | Terminated | 27 Nov 2019 |
| F-0177-2020 | pH-FX 4 fl. oz. plastic bottle, SKU: 100-1A | N/A | Class II | Terminated | 27 Nov 2019 |
| F-0178-2020 | SlimUp 60 capsules per plastic bottle, SKU: 100-5B | N/A | Class II | Terminated | 27 Nov 2019 |
| F-0179-2020 | AquaLyte, 30g pkg./foil pouch, SKU: 1023 | N/A | Class II | Terminated | 27 Nov 2019 |
| F-0180-2020 | Body Mass Reset, 4 fl. oz. plastic bottle, SKU: 100-8C | N/A | Class II | Terminated | 27 Nov 2019 |
| F-0181-2020 | GH-C, 60 capsules per plastic bottle, SKU: 100-4F | N/A | Class II | Terminated | 27 Nov 2019 |
| F-0182-2020 | Q-min, 50 capsules per plastic bottle, SKU: 100-9B | N/A | Class II | Terminated | 27 Nov 2019 |
| F-1239-2020 | Dino Min, 60 capsules per plastic bottle, SKU: 100-1C | N/A | Class II | Terminated | 27 Nov 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
- 14Median of the firm: 11
- Events of the firm on the register
- 3
Other events of the firm
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 18 Oct 2019 | Energy FX: a) original Aluminum (100-3A) b) sleek (adult and kid & pet) (100-3B) | Device | Class II | 1 |
| 18 Oct 2019 | Basic Reset Earth Wash Cleaner and Personal Care, Eco Friendly, Non Toxic, 2 fl.oz. bottle, Distributed by: Basic Reset | Drug | Class II | 11 |
Official channels
- FDA enforcement report F-0170-2020The 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 83917. https://recallregister.com/fda/ii/83917/. 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:
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,…
- What quantity of product is in FDA event 83917?
- The event has 14 product records. The first record gives this quantity:
262 bottles
- How did the recall start?
- The FDA record says:
FDA Mandated
- How many food recalls of 2019 have the same class?
- 56% of the 516 food events that started in 2019 are in Class II.