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Basic Reset Inc.

14 recall records on file.

2019

14 records

Class IITerminatedRecall F-0170-2020

Product description

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

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

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Event ID
83917
Code info
1820705, 1806004, 1733404, 1815204, 1719204, W0002670, W0000304, W000325, W0003878
Product quantity
262 bottles
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.
Voluntary / mandated
FDA Mandated
Initial firm notification
E-Mail
Product type
Food
Recalling firm location
260 W Main St Ste 103, N/A, Hendersonville, TN, United States
Recall initiation date
09/23/2019
Center classification date
11/21/2019
Termination date
08/19/2020
Class IITerminatedRecall F-0171-2020

Product description

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

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

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Event ID
83917
Code info
ACRXI, ADMUA
Product quantity
2465 bottles
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.
Voluntary / mandated
FDA Mandated
Initial firm notification
E-Mail
Product type
Food
Recalling firm location
260 W Main St Ste 103, N/A, Hendersonville, TN, United States
Recall initiation date
09/23/2019
Center classification date
11/21/2019
Termination date
08/19/2020
Class IITerminatedRecall F-0172-2020

Product description

Vibrant ENERGY DRINK 450 g plastic canister 100-4A

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

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Event ID
83917
Code info
01190P06576
Product quantity
1980 canisters
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.
Voluntary / mandated
FDA Mandated
Initial firm notification
E-Mail
Product type
Food
Recalling firm location
260 W Main St Ste 103, N/A, Hendersonville, TN, United States
Recall initiation date
09/23/2019
Center classification date
11/21/2019
Termination date
08/19/2020
Class IITerminatedRecall F-0173-2020

Product description

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

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

View full record
Event ID
83917
Code info
F1246L and P12317
Product quantity
6887 cases
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.
Voluntary / mandated
FDA Mandated
Initial firm notification
E-Mail
Product type
Food
Recalling firm location
260 W Main St Ste 103, N/A, Hendersonville, TN, United States
Recall initiation date
09/23/2019
Center classification date
11/21/2019
Termination date
08/19/2020
Class IITerminatedRecall F-0174-2020

Product description

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

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

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Event ID
83917
Code info
ZCBEEPF1881, 2018061, 2018105, ZCBEEPG2935, ZCBEEPG3724
Product quantity
N/A
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.
Voluntary / mandated
FDA Mandated
Initial firm notification
E-Mail
Product type
Food
Recalling firm location
260 W Main St Ste 103, N/A, Hendersonville, TN, United States
Recall initiation date
09/23/2019
Center classification date
11/21/2019
Termination date
08/19/2020
Class IITerminatedRecall F-0175-2020

Product description

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

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

View full record
Event ID
83917
Code info
29049,28343,27618A,19018B, 35317B,101617,08518A, 29123
Product quantity
N/A
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.
Voluntary / mandated
FDA Mandated
Initial firm notification
E-Mail
Product type
Food
Recalling firm location
260 W Main St Ste 103, N/A, Hendersonville, TN, United States
Recall initiation date
09/23/2019
Center classification date
11/21/2019
Termination date
08/19/2020
Class IITerminatedRecall F-0176-2020

Product description

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

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

View full record
Event ID
83917
Code info
180209-BSC2354, 170801-BSC2354
Product quantity
N/A
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.
Voluntary / mandated
FDA Mandated
Initial firm notification
E-Mail
Product type
Food
Recalling firm location
260 W Main St Ste 103, N/A, Hendersonville, TN, United States
Recall initiation date
09/23/2019
Center classification date
11/21/2019
Termination date
08/19/2020
Class IITerminatedRecall F-0177-2020

Product description

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

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

View full record
Event ID
83917
Code info
29031,28231,28335,28175, 28057, 80324, 29119
Product quantity
N/A
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.
Voluntary / mandated
FDA Mandated
Initial firm notification
E-Mail
Product type
Food
Recalling firm location
260 W Main St Ste 103, N/A, Hendersonville, TN, United States
Recall initiation date
09/23/2019
Center classification date
11/21/2019
Termination date
08/19/2020
Class IITerminatedRecall F-0178-2020

Product description

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

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

View full record
Event ID
83917
Code info
170801-BSC2130
Product quantity
N/A
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.
Voluntary / mandated
FDA Mandated
Initial firm notification
E-Mail
Product type
Food
Recalling firm location
260 W Main St Ste 103, N/A, Hendersonville, TN, United States
Recall initiation date
09/23/2019
Center classification date
11/21/2019
Termination date
08/19/2020
Class IITerminatedRecall F-0179-2020

Product description

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

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

View full record
Event ID
83917
Code info
91117
Product quantity
N/A
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.
Voluntary / mandated
FDA Mandated
Initial firm notification
E-Mail
Product type
Food
Recalling firm location
260 W Main St Ste 103, N/A, Hendersonville, TN, United States
Recall initiation date
09/23/2019
Center classification date
11/21/2019
Termination date
08/19/2020
Class IITerminatedRecall F-0180-2020

Product description

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

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

View full record
Event ID
83917
Code info
40517
Product quantity
N/A
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.
Voluntary / mandated
FDA Mandated
Initial firm notification
E-Mail
Product type
Food
Recalling firm location
260 W Main St Ste 103, N/A, Hendersonville, TN, United States
Recall initiation date
09/23/2019
Center classification date
11/21/2019
Termination date
08/19/2020
Class IITerminatedRecall F-0181-2020

Product description

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

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

View full record
Event ID
83917
Code info
71917, GH7-17
Product quantity
N/A
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.
Voluntary / mandated
FDA Mandated
Initial firm notification
E-Mail
Product type
Food
Recalling firm location
260 W Main St Ste 103, N/A, Hendersonville, TN, United States
Recall initiation date
09/23/2019
Center classification date
11/21/2019
Termination date
08/19/2020
Class IITerminatedRecall F-0182-2020

Product description

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

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

View full record
Event ID
83917
Code info
170801-BSC0462
Product quantity
N/A
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.
Voluntary / mandated
FDA Mandated
Initial firm notification
E-Mail
Product type
Food
Recalling firm location
260 W Main St Ste 103, N/A, Hendersonville, TN, United States
Recall initiation date
09/23/2019
Center classification date
11/21/2019
Termination date
08/19/2020
Class IITerminatedRecall F-1239-2020

Product description

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

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

View full record
Event ID
83917
Code info
02219A, 27418A, 22618B, 18919A, 11618B, 07819A, 06118D, 36017B
Product quantity
N/A
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.
Voluntary / mandated
FDA Mandated
Initial firm notification
E-Mail
Product type
Food
Recalling firm location
260 W Main St Ste 103, N/A, Hendersonville, TN, United States
Recall initiation date
09/23/2019
Center classification date
11/21/2019
Termination date
08/19/2020