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Basic Reset Inc.

10 recall records in Other.

2019

10 records

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.

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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.

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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.

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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.

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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.

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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.

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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