Food Recall Check
Class I · High risk Terminated Initiated May 13, 2026 (5 months ago)

Pearl Milling Company Original Pancake & Waffle Mix Complete recall

Recalled by Cereles En General Sas · Santo Domingo, N/A, Dominican Republic (the)

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Undeclared allergens: Milk and Soy

Undeclared allergens: Milk Soy

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Pearl Milling Company Original Pancake & Waffle Mix Complete (Mezcla Para Panqueques y Waffles) Net Wt 5.99 oz (170 g). Packed in 50 - 5.99 oz BOPP Pouch units per master case. Keep in a cool, dry place.

Quantity: 25,450 individual retail units

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot Codes:23A26C6, 24A26A7, 24A26B2, 24A26B5, 24A26A7, 24A26C6, 23A26B5, 24A26A6, 25B26C13, 25B26A14, 25B26B4, 25B26A15, 25B26B1 Expiration Date (s): 01/23/2027 ,01/24/2027 and 02/25/2027

Where it was sold

Puerto Rico

FDA's distribution note: Distributed only in Puerto Rico

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk, soy; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Cereles En General Sas
Initiated by
Voluntary: Firm initiated
Recall initiated
May 13, 2026
In FDA report of
Jul 1, 2026
Terminated
Aug 14, 2026
FDA recall number
H-1124-2026 · event 99118
Official record
FDA enforcement report search