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ACTIVE RECALL — CLASS IIActive recallH-0674-2026/FDA enforcement
Marquez Brothers International, INC.·Food·Apr 7, 2026

El Mexicano Agua Fresca De Horchata Instant Horchata Drink NET WT 12oz (340g) Ingredients: ***…

What you need to know

Class II

  • What happened

    Undeclared milk.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Active recall · classified by the FDAAK, AL, AR, AZ +25 moreMore food

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Product identification

Source: FDA FOOD

Brand nameMarquez Brothers International, INC.
Recalling firmMarquez Brothers International, INC.Fresno, CA, United States
UPC / barcodes
0 42743 19020 4
Lot / date codes
  • Lot, Expiration: HR02324, 01/26/26; HR02324, 01/29/26; HR06424, 03/07/26; HR09924, 04/09/26; HR10024, 04/10/26; HR12924, 05/09/26
  • HR13024, 05/13/26; HR13024, 05/14/26; HR16424, 06/13/26; HR17824, 06/27/26; HR17824, 06/28/26; HR21124, 07/30/26
Distribution area
AKALARAZCACOFLIAIDILINKSLAMIMNMOMTNENMNVOHOKORTNTXUTVAWAWI

Domestic distribution: AK, AL, AR, AZ, CA, CO, FL, IA, ID, IL, IN, KS, LA, MI, MN, MO, MT, NE, NM, NV, OH, OK, OR, TN, TX, UT, VA, WA, WI. Foreign distribution: Canada, Japan.

United States, Canada, Japan

Quantity affected405, 136 packages (16 packages/case; 25, 321 cases)
Recall initiationFDA report date: April 29, 2026
FDA recall numberH-0674-2026

Beyond the headline

The recall, in context

Marquez Brothers International, INC. initiated this food recall on April 7, 2026. The FDA enforcement report states: Undeclared milk. The FDA report lists distribution as: Domestic distribution: AK, AL, AR, AZ, CA, CO, FL, IA, ID, IL, IN, KS, LA, MI, MN, MO, MT, NE, NM, NV, OH, OK, OR, TN, TX, UT, VA, WA, WI. Foreign distribution: Canada, Japan.

The FDA enforcement report describes the reason as: Undeclared milk.

El Mexicano Agua Fresca De Horchata Instant Horchata Drink NET WT 12oz (340g) Ingredients: ***… was made or distributed by Marquez Brothers International, INC. in Fresno, CA, United States. This page reflects FDA report H-0674-2026, dated April 29, 2026.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared milk

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a milk allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed cow's milk allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a milk allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the El Mexicano Agua Fresca De Horchata Instant Horchata Drink NET WT 12oz (340g) Ingredients: ***… recall?

Marquez Brothers International, INC. recalled El Mexicano Agua Fresca De Horchata Instant Horchata Drink NET WT 12oz (340g) Ingredients: ***… in an FDA Class II enforcement action reported as H-0674-2026. Undeclared milk.

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have a milk allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Marquez Brothers International, INC. recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-0674-2026. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Marquez Brothers International, INC.

View brand
Class II·

Marquez Brothers International, INC.

El Mexicano Horchata Casera Instant Horchata Drink NET WT 14oz (396g) Ingredients: *** Milk…

Undeclared milk.

AK, AL, AR +26 more +2 countriesFood
Class II·

Marquez Brothers International, INC.

Bulk Horchata Powder 3951 (100547) 1/25 Horchata

Undeclared milk.

AK, AL, AR +26 more +2 countriesFood

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.