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Class II: temporary or reversible health riskTerminated

Basic Reset Body Mass Reset Recall

Body Mass Reset, 4 fl

Basic Reset Inc. · Hendersonville, TN

Risk level
Class II
Reported by FDA
Nov 27, 2019
Recall ID
F-0180-2020
Check your lot numberHow we source this data

Summary

Basic Reset recalled Body Mass Reset starting Sep 23, 2019. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0180-2020 on Nov 27, 2019. Reason: Products do not conform to Dietary Supplement CGMP regulations. Status: Terminated.

Why it was recalled

Products do not conform to Dietary Supplement CGMP regulations.

Product description

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

Lot numbers, UPCs & expiration codes

40517

Where it was sold

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.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0180-2020
Classification
Class II
Status
Terminated
Recall initiated
Sep 23, 2019
FDA report date
Nov 27, 2019
Quantity
N/A
Recall type
FDA Mandated
Recalling firm
Basic Reset Inc.

Original FDA data

Every field from FDA enforcement report F-0180-2020, exactly as published.

Show all FDA fields
City
Hendersonville
State
TN
Status
Terminated
Country
United States
Event ID
83917
Address
260 W Main St Ste 103
Code information
40517
Postal code
37075-7316
Report date
Nov 27, 2019
Product type
Food
Recall number
F-0180-2020
Classification
Class II
Recalling firm
Basic Reset Inc.
Termination date
Aug 19, 2020
Reason for recall
Products do not conform to Dietary Supplement CGMP regulations.
Voluntary / mandated
FDA Mandated
Product description
Body Mass Reset, 4 fl. oz. plastic bottle, SKU: 100-8C
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.
Recall initiation date
Sep 23, 2019
Initial firm notification
E-Mail
Center classification date
Nov 21, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0180-2020, published Nov 27, 2019. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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