Basic Reset Inc. Recall: Products do not conform to Dietary Supplement CGMP regulations.

🇺🇸 United States

1. September 23, 2019 - Recall initiated
2. November 27, 2019 - Reported by source
3. August 19, 2020 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0177-2020

Event ID

83917

Status

Terminated

Classification

Class II

Company

Basic Reset Inc.

Product description

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

Quantity

N/A

Reason

Products do not conform to Dietary Supplement CGMP regulations.

Recall initiation date

September 23, 2019

Report date

November 27, 2019

Classification date

Not published in this source record

Termination date

August 19, 2020

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.

UPC, lot, and code information

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

Voluntary or mandated

FDA Mandated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 83917 with 9 other product entries in Public Health Trace.

Responsible company: Basic Reset Inc.

Other recalls from Basic Reset Inc.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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