Class IIFood recall: undeclared milk
Bulk Horchata Powder and 2 more products
Marquez Brothers International, Inc., of Fresno, CA, began recalling these 3 products on . FDA classified the recall as Class II on .
Why it was recalled
In FDA’s words:
Undeclared milk.
The allergen tags on this page are ours, matched from FDA’s words above.
The 3 products
Bulk Horchata Powder
Bulk Horchata Powder 3951 (100547) 1/25 HORCHATA UPC: 042743-19015-0 Item: 100547
- Codes and dates
- Lot, Expiration: HR02224, 01/23/26; HR06124, 03/05/26; HR16524, 06/14/26; HR23624, 08/27/26; HR34124, 12/11/26; HR07125, 03/13/27; HR09025, 04/03/27; HR23425, 08/27/27; HR34425, 12/15/27; HR01926, 01/28/28.
- Quantity
- 2,494 cases (25 lbs/case)
- Class
- Class II
- Recall number
- H-0672-2026
EL MEXICANO horchata casera Instant Horchata Drink
EL MEXICANO horchata casera Instant Horchata Drink NET WT 14oz (396g) INGREDIENTS: *** MILK SUBSTITUTE (WHEY *** LACTOSE *** DISTRIBUTED BY MARQUEZ BROTHERS INTERNATIONAL, INC. San Jose CA 95138 UPC: 042743190266 Item: 102284
- Codes and dates
- Lot, Expiration: HC10124, 04/11/26; HC16524, 06/14/26; HC21324, 08/01/26; HC29924, 10/28/26; HC06625, 03/06/27; HC06625, 03/07/27; HC16325, 06/13/27; HC19525, 07/15/27; HC28325, 10/13/27; HC28325, 10/14/27.
- Quantity
- 40,032 packages (16 packages/case; 2,502 cases)
- Class
- Class II
- Recall number
- H-0673-2026
EL MEXICANO agua fresca de horchata Instant Horchata Drink
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
- Codes and dates
- 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.
- Quantity
- 405,136 packages (16 packages/case; 25,321 cases)
- Class
- Class II
- Recall number
- H-0674-2026
Where it was distributed
In FDA’s words:
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.
What Class II means
In FDA’s definitions, a Class II recall is one where: use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse health consequences is remote. FDA’s recall definitions
If you have this product
- FDA’s enforcement report doesn’t say what to do with a recalled product. FDA posts some companies’ recall announcements on its Recalls, Market Withdrawals and Safety Alerts page; not every recall has one.
- FDA doesn’t update a recall’s status after classifying it, so this page can’t tell you whether the recall is still open.
- If someone has a serious allergic reaction, call 911. Signs of a serious reaction
Source
FDA’s Enforcement Report, read through openFDA. This recall first appeared in the report of . openFDA asks that its data not be relied on for decisions about medical care. AllergyNest isn’t affiliated with or endorsed by FDA.