CLASS II Food recall · Reported 15 Oct 2025 · FDA Enforcement Report

Gluta Plus (Glutathione)/container recalled by New Spirit Naturals

New Spirit Naturals is recalling Gluta Plus (Glutathione)/container. The recall was initiated on 3 Sep 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot codes: 231101V; 231142V; 241773V; 243381V
Quantity recalled83 units

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
H-0020-2026
FDA event ID
97569
Recalling firm
New Spirit Naturals, San Dimas, CA
Classification
Class II
Status
Terminated
Recall initiated
3 Sep 2025
FDA classified
6 Oct 2025
Reported
15 Oct 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Undeclared Milk
Product category
Dietary Supplements

Timeline

3 Sep 2025Recall initiated by company
6 Oct 2025Classified by FDA+33 days
15 Oct 2025Published in enforcement report+9 days

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

Reason for recall

undeclared allergen ingredient Milk.

Product as listed by the FDA

Gluta Plus (Glutathione) 60 capsules/container. UPC: NA

Where it was distributed

Products are sold directly to consumers via firm's online website.

Stores named: Online Retailers

Questions about this recall

Is Gluta Plus (Glutathione)/container recalled?

Yes. New Spirit Naturals recalled Gluta Plus (Glutathione)/container on 3 Sep 2025. The recall is Class II and its status is Terminated. Recall number H-0020-2026.

Why was it recalled?

undeclared allergen ingredient Milk.

Which lots are affected?

Lot codes: 231101V; 231142V; 241773V; 243381V

Where was it sold?

Products are sold directly to consumers via firm's online website.

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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