HIGH

New Spirit Naturals Recalls Gluta Plus Capsules Over Milk Allergen

New Spirit Naturals recalled 83 units of Gluta Plus (Glutathione) on September 3, 2025, due to undeclared milk allergens. The recall affects specific lot codes and poses a high risk to consumers with milk allergies. This recall is active, and consumers should stop using the product immediately.

Quick Facts at a Glance

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

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

Product Details

The recall involves Gluta Plus (Glutathione) sold in 60-capsule containers. Affected lot codes are 231101V, 231142V, 241773V, and 243381V. Products were sold directly to consumers via the firm's online website.

The Hazard

The product contains milk, an undeclared allergen. This poses a serious risk to individuals with milk allergies, potentially leading to severe allergic reactions.

Reported Incidents

No incidents or injuries have been reported related to this recall. However, the undeclared allergen could cause serious health risks for allergic individuals.

What to Do

Consumers should not consume the recalled product. Contact New Spirit Naturals Inc. for refund or replacement information.

Contact Information

For more details, consumers can visit the FDA’s website or contact New Spirit Naturals Inc. directly for assistance.

Key Facts

  • Product: Gluta Plus (Glutathione)
  • Quantity recalled: 83 units
  • Recall date: September 3, 2025
  • Hazard: Undeclared milk allergen
  • Class II recall

Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeGlutathione Capsules
Sold At
Multiple Retailers

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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