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Class II: temporary or reversible health riskTerminated

Basic Reset pH-FX 4 fl Recall

pH-FX 4 fl

Basic Reset Inc. · Hendersonville, TN

Risk level
Class II
Reported by FDA
Nov 27, 2019
Recall ID
F-0177-2020
Check your lot numberHow we source this data

Summary

Basic Reset recalled pH-FX 4 fl starting Sep 23, 2019. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0177-2020 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

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

Lot numbers, UPCs & expiration codes

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

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-0177-2020
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-0177-2020, 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
29031,28231,28335,28175, 28057, 80324, 29119
Postal code
37075-7316
Report date
Nov 27, 2019
Product type
Food
Recall number
F-0177-2020
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
pH-FX 4 fl. oz. plastic bottle, SKU: 100-1A
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-0177-2020, published Nov 27, 2019. View the source record (openFDA) · FDA enforcement reports

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

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