FDA recall, , Moderate risk
El Mexicano Horchata Drinks
Bulk Horchata Powder has undeclared milk.
Summary by Recall Canary from the FDA notice
What happened
Marquez Brothers International, Inc. of Fresno, California, recalled El Mexicano agua fresca de horchata Instant Horchata Drink, Bulk Horchata Powder 3951, and El Mexicano horchata casera Instant Horchata Drink because they contain undeclared milk. The company began the recall on April 7, 2026, and the FDA added it to its Enforcement Report on April 23, 2026. The products were distributed domestically in 29 states and internationally to Canada and Japan.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for food recalls:
- Return it to the store where you bought it, or throw it away.
- Don't give it to anyone else, such as a food bank, or to a pet.
Is yours affected?
3 products
Match the lot code and UPC listed under your product.
A UPC is the number printed under a barcode.
El Mexicano agua fresca de horchata Instant Horchata Drink Net wt 12oz (340g) Ingredients: *** Milk Substitute (WHEY *** Lactose ***
- UPC
- 042743190204
- Lot code
- HR02324
Bulk Horchata Powder 3951 (100547) 1/25 Horchata
- UPC
- 042743-19015-0
- Lot code
- HR02224
El Mexicano horchata casera Instant Horchata Drink Net wt 14oz (396g) Ingredients: *** Milk Substitute (WHEY *** Lactose ***
- UPC
- 042743190266
- Lot code
- HC10124
Recall details
- Company began the recall
- Sold in
Domestic distribution: Alaska, Alabama, Arkansas, Arizona, California, Colorado, Florida, Iowa, Idaho, Illinois, Indiana, Kansas, Louisiana, Michigan, Minnesota, Missouri, Montana, Nebraska, New Mexico, Nevada, Ohio, Oklahoma, Oregon, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin. Foreign distribution: Canada, Japan.
- Company
- Marquez Brothers International, Inc.Fresno, California
- Hazard
- Undeclared milk
- Risk
Moderate risk
Eating it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98761
- Recall numbers
- H-0672-2026 to H-0674-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
