HIGHFDA FOOD

New Spirit Naturals Gluta Plus Glutathione 60-Capsule Recall for Milk Allergy Hazard

New Spirit Naturals Inc. recalls Gluta Plus glutathione in 60-capsule containers sold online after undeclared milk allergen found. The recall is Class II with 83 units affected. Consumers should stop using the product and contact the company for refunds or replacements.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA FOOD
Recall date
September 3, 2025
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
September 3, 2025
Hazard Level
HIGH
Brand
New Spirit Naturals
Category
Food & Beverages
At-Risk Groups
GENERAL, PREGNANT, PETS

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Food Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
New Spirit Naturals
Product type
Glutathione supplement
Model numbers
231101V, 231142V, 241773V, 243381V
Sizes
60 capsules/container

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    September 3, 2025

  2. Reported by FDA FOOD

    October 15, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

undeclared allergen ingredient Milk.

What You Should Do

Consumers who have purchased this product should not consume it. Contact New Spirit Naturals Inc. for refund or replacement information. Notification method: Letter

About This Product

Gluta Plus is a dietary supplement marketed to support glutathione levels. Consumers buy it for wellness purposes.

Why This Is Dangerous

The undeclared milk allergen can trigger allergic reactions in milk-allergic individuals, which can be severe.

Industry Context

This recall is not described as part of a broader industry pattern.

Real-World Impact

Consumers must avoid this product to prevent allergic reactions; refunds or replacements offer a remedy.

Practical Guidance

How to identify if yours is affected

  1. Check if your container has model numbers 231101V, 231142V, 241773V, or 243381V.
  2. Confirm label does not indicate milk allergen as an undeclared ingredient.
  3. Verify purchase was via the firm’s online store.

Where to find product info

Refer to the FDA enforcement page linked in the recall notice for official details.

What timeline to expect

Refunds or replacements via letter notification are anticipated; specific timelines are not provided.

If the manufacturer is unresponsive

  • Document all communications with New Spirit Naturals Inc.
  • Contact FDA CPSC if company is unresponsive.

How to prevent similar issues

  • Choose supplements with complete ingredient labeling.
  • Look for allergen statements on labels and verify before purchase.
  • Keep purchase records and packaging until issue is resolved.

Documentation advice

Retain packaging, receipts, and all correspondence related to the recall.

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Product Details

Brand: New Spirit Naturals. Product: Gluta Plus Glutathione, 60 capsules per container. UPC: Not available. Model numbers: 231101V, 231142V, 241773V, 243381V. Quantity: 83 units. Distribution: Sold directly to consumers via firm’s online website.

Reported Incidents

No specific injuries or incidents are detailed in the recall notice.

Key Facts

  • 83 total units recalled
  • Milk allergen undeclared
  • 60 capsules per container
  • Models: 231101V, 231142V, 241773V, 243381V
  • Notification by letter

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERALPREGNANTPETSPREGNANT
Injury Types
POISONINGELECTRICALOTHER

Product Details

Model Numbers
231101V
231142V
241773V
243381V
Report Date
October 15, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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