Gluta Plus (Glutathione) 60 capsules/container.
Recalling firm: New Spirit Naturals Inc.
Why it was recalled
undeclared allergen ingredient Milk.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Apr 23, 2026.
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ProductGluta Plus (Glutathione) 60 capsules/container. UPC: NA
FDA code information
Lot codes: 231101V; 231142V; 241773V; 243381V
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Full FDA record and distribution details
Original product description
Gluta Plus (Glutathione) 60 capsules/container. UPC: NA
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| lot | 231101V | Lot codes: 231101V; 231142V; 241773V; 243381V |
| lot | 231142V | Lot codes: 231101V; 231142V; 241773V; 243381V |
| lot | 241773V | Lot codes: 231101V; 231142V; 241773V; 243381V |
| lot | 243381V | Lot codes: 231101V; 231142V; 241773V; 243381V |
Original FDA recall reason
undeclared allergen ingredient Milk.
Recall details
- Recall number
- H-0020-2026
- Event ID
- 97569
- FDA status
- Terminated
- Initiated
- Sep 3, 2025
- Reported
- Oct 15, 2025
- Classified
- Oct 6, 2025
- Terminated
- Apr 23, 2026
- Quantity
- 83 units
- Location
- San Dimas, CA, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
Products are sold directly to consumers via firm's online website.
FDA source record · H-0020-2026
Data updated September 16, 2026. View official FDA data ↗
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