FDA Recall United States Ongoing 2026 recordClass II
Marquez Brothers International, Inc.
- Product
- EL MEXICANO horchata casera Instant Horchata Drink NET WT 14…
- Published
- April 29, 2026
- Distribution
- Domestic distribution: AK, AL, AR, AZ, C…
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Policy version 2026-07-21, effective July 21, 2026.
United States
OngoingClass II
Undeclared milk.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| EL MEXICANO agua fresca de horchata Instant Horchata Drink NET WT 12oz (340g) INGREDIENTS: *** MILK SUBSTITUTE (WHEY *** LACTOSE *** DISTRIBUTED BY MARQUEZ BROTHERS INTERNATIONAL, INC. San Jose CA 95138 UPC: 042743190204 Item: 102279 | 042743190204 | 405,136 packages (16 packages/case; 25,321 cases) | 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; HR21224, 07/31/26; HR23524, 08/26/26; HR23624, 08/27/26; HR26724, 09/25/26; HR29724, 10/24/26; HR29824, 10/25/26; HR29924, 11/19/26; HR32424, 11/20/26; HR02225, 01/23/27; HR02225, 01/24/27; HR05825, 03/05/27; HR05925, 03/06/27; HR08625, 03/28/27; HR08625, 03/31/27; HR08725, 04/01/27; HR15725, 06/09/27; HR16025, 06/10/27; HR16225, 06/12/27; HR16325, 06/13/27; HR19125, 07/11/27; HR19225, 07/15/27; HR23325, 08/22/27; HR23225, 08/21/27; HR27925, 10/08/27; HR28225, 10/13/27; HR34425, 12/15/27; HR34525, 12/16/27. |
This recall shares FDA event ID 98761 with 2 other product entries in Public Health Trace.
FDA Recall United States Ongoing 2026 recordClass II
FDA Recall United States Ongoing 2026 recordClass II
Responsible company: Marquez Brothers International, Inc.
FDA Recall United States Ongoing 2026 recordClass II
FDA Recall United States Ongoing 2026 recordClass II
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Alaska | 1 |
| Alabama | 1 |
| Arkansas | 1 |
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Florida | 1 |
| Iowa | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Louisiana | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| Missouri | 1 |
| Montana | 1 |
| Nebraska | 1 |
| New Mexico | 1 |
| Nevada | 1 |
| Ohio | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| Tennessee | 1 |
| Texas | 1 |
| Utah | 1 |
| Virginia | 1 |
| Washington | 1 |
| Wisconsin | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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