FDA recall record

Healthwest Minerals, Inc. dba Mt. Capra Products Mt recall — FDA F-1347-2024

The Goat Milk Formula Recipe Kit has been sold and marketed as infant formula, but product has not submitted to FDA the premarket notification required…

Class Iclassification
F-1347-2024official record ID
Jun 19, 2024report date

Recall record at a glance

Official recordF-1347-2024
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmHealthwest Minerals, Inc. dba Mt. Capra Products
Report dateJun 19, 2024
Recall initiation dateMay 10, 2024
Quantity1506 boxes
LocationChehalis, WA, United States

Official product description

Mt. Capra Goat Milk Formula Recipe Kit (net wt. 10lbs. 8oz.) and Bundle Refill. Each Goat Milk Formula Recipe Kit consist of 10 individually packaged ingredients: *Whole Goat Milk *Goat Milk Lactose *Goat Milk Ghee -Extra Virgin Olive Oil -Expeller-Pressed Grapeseed Oil -Unsulphured, Blackstrap Molasses -Head Start Multivitamin Powder -Goat Milk Colostrum -Flora Start Kids Probiotics -Nordic Natural DHA Infants Bundle Refill consists of three individually packaged ingredients: *Whole Goat Milk *Goat Milk Lactose *Goat Milk Ghee

Why the product was recalled

The Goat Milk Formula Recipe Kit has been sold and marketed as infant formula, but product has not submitted to FDA the premarket notification required for an infant formula for review.

Distribution information

nationwide

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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