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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 83917

14 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
September 23, 2019
Product types
Food
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Basic Reset Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

14 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 14

BETA FACTOR DIETARY SUPPLEMENT 60 capsules per plastic bottle, SKU: 100-4F

F-0170-2020
Recall number
F-0170-2020
Initiated
September 23, 2019
Classification
Class II
Status
Terminated
Recalling firm
Basic Reset Inc.
Quantity
262 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not conform to Dietary Supplement CGMP regulations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

Code information

1820705, 1806004, 1733404, 1815204, 1719204, W0002670, W0000304, W000325, W0003878

Distribution pattern

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.

food · product 2 of 14

TRIM UP DIETARY SUPPLEMENT 80 capsules per plastic bottle, SKU: 100-5A

F-0171-2020
Recall number
F-0171-2020
Initiated
September 23, 2019
Classification
Class II
Status
Terminated
Recalling firm
Basic Reset Inc.
Quantity
2465 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not conform to Dietary Supplement CGMP regulations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

Code information

ACRXI, ADMUA

Distribution pattern

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.

food · product 3 of 14

Vibrant ENERGY DRINK 450 g plastic canister 100-4A

F-0172-2020
Recall number
F-0172-2020
Initiated
September 23, 2019
Classification
Class II
Status
Terminated
Recalling firm
Basic Reset Inc.
Quantity
1980 canisters

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not conform to Dietary Supplement CGMP regulations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

Code information

01190P06576

Distribution pattern

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.

food · product 4 of 14

Vibrant ENERGY DRINK 15 g foil pouches (15 pack case) 100-4A and 100-4B

F-0173-2020
Recall number
F-0173-2020
Initiated
September 23, 2019
Classification
Class II
Status
Terminated
Recalling firm
Basic Reset Inc.
Quantity
6887 cases

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not conform to Dietary Supplement CGMP regulations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

Code information

F1246L and P12317

Distribution pattern

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.

food · product 5 of 14

Bee Gold 8oz. pkg./plastic pouch, SKU: 100-4C

F-0174-2020
Recall number
F-0174-2020
Initiated
September 23, 2019
Classification
Class II
Status
Terminated
Recalling firm
Basic Reset Inc.
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not conform to Dietary Supplement CGMP regulations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

Code information

ZCBEEPF1881, 2018061, 2018105, ZCBEEPG2935, ZCBEEPG3724

Distribution pattern

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.

food · product 6 of 14

Ionyte 4 fl. oz. plastic bottle, SKU: 100-1B

F-0175-2020
Recall number
F-0175-2020
Initiated
September 23, 2019
Classification
Class II
Status
Terminated
Recalling firm
Basic Reset Inc.
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not conform to Dietary Supplement CGMP regulations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

Code information

29049,28343,27618A,19018B, 35317B,101617,08518A, 29123

Distribution pattern

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.

food · product 7 of 14

Mello-Tonin 2 fl. oz. glass bottle, SKU: 100-5C

F-0176-2020
Recall number
F-0176-2020
Initiated
September 23, 2019
Classification
Class II
Status
Terminated
Recalling firm
Basic Reset Inc.
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not conform to Dietary Supplement CGMP regulations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

Code information

180209-BSC2354, 170801-BSC2354

Distribution pattern

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.

food · product 8 of 14

pH-FX 4 fl. oz. plastic bottle, SKU: 100-1A

F-0177-2020
Recall number
F-0177-2020
Initiated
September 23, 2019
Classification
Class II
Status
Terminated
Recalling firm
Basic Reset Inc.
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not conform to Dietary Supplement CGMP regulations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

Code information

29031,28231,28335,28175, 28057, 80324, 29119

Distribution pattern

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.

food · product 9 of 14

SlimUp 60 capsules per plastic bottle, SKU: 100-5B

F-0178-2020
Recall number
F-0178-2020
Initiated
September 23, 2019
Classification
Class II
Status
Terminated
Recalling firm
Basic Reset Inc.
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not conform to Dietary Supplement CGMP regulations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

Code information

170801-BSC2130

Distribution pattern

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.

food · product 10 of 14

AquaLyte, 30g pkg./foil pouch, SKU: 1023

F-0179-2020
Recall number
F-0179-2020
Initiated
September 23, 2019
Classification
Class II
Status
Terminated
Recalling firm
Basic Reset Inc.
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not conform to Dietary Supplement CGMP regulations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

Code information

91117

Distribution pattern

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.

food · product 11 of 14

Body Mass Reset, 4 fl. oz. plastic bottle, SKU: 100-8C

F-0180-2020
Recall number
F-0180-2020
Initiated
September 23, 2019
Classification
Class II
Status
Terminated
Recalling firm
Basic Reset Inc.
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not conform to Dietary Supplement CGMP regulations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

Code information

40517

Distribution pattern

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.

food · product 12 of 14

GH-C, 60 capsules per plastic bottle, SKU: 100-4F

F-0181-2020
Recall number
F-0181-2020
Initiated
September 23, 2019
Classification
Class II
Status
Terminated
Recalling firm
Basic Reset Inc.
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not conform to Dietary Supplement CGMP regulations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

Code information

71917, GH7-17

Distribution pattern

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.

food · product 13 of 14

Q-min, 50 capsules per plastic bottle, SKU: 100-9B

F-0182-2020
Recall number
F-0182-2020
Initiated
September 23, 2019
Classification
Class II
Status
Terminated
Recalling firm
Basic Reset Inc.
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not conform to Dietary Supplement CGMP regulations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

Code information

170801-BSC0462

Distribution pattern

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.

food · product 14 of 14

Dino Min, 60 capsules per plastic bottle, SKU: 100-1C

F-1239-2020
Recall number
F-1239-2020
Initiated
September 23, 2019
Classification
Class II
Status
Terminated
Recalling firm
Basic Reset Inc.
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Products do not conform to Dietary Supplement CGMP regulations.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

Code information

02219A, 27418A, 22618B, 18919A, 11618B, 07819A, 06118D, 36017B

Distribution pattern

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.