CLASS II Food recall · Reported 27 Nov 2019 · FDA Enforcement Report

AquaLyte pkg recalled by Basic Reset

Basic Reset is recalling AquaLyte pkg, distributed nationwide in the US. The recall was initiated on 23 Sep 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes91117

Quantity recalledN/A

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-0179-2020
FDA event ID: 83917
Recalling firm: Basic Reset, Hendersonville, TN
Brand: AquaLyte
Classification: Class II
Status: Terminated
Recall initiated: 23 Sep 2019
FDA classified: 21 Nov 2019
Reported: 27 Nov 2019
Type: FDA Mandated
Customers notified by: E-Mail
Reason category: Manufacturing (CGMP) Deviations
Product category: Other

Timeline

23 Sep 2019	Recall initiated by company
21 Nov 2019	Classified by FDA	+59 days
27 Nov 2019	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Products do not conform to Dietary Supplement CGMP regulations.

Product as listed by the FDA

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

Where it was distributed

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.

Nationwide Puerto Rico

Questions about this recall

Is AquaLyte pkg recalled?

Yes. Basic Reset recalled AquaLyte pkg on 23 Sep 2019. The recall is Class II and its status is Terminated. Recall number F-0179-2020.

Why was it recalled?

Products do not conform to Dietary Supplement CGMP regulations.

Which lots are affected?

91117

Where was it sold?

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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