← FDA ENFORCEMENT
F-1750-2024Class I

Prime Food Processing Corp.

Recalling firm
Prime Food Processing Corp.
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2024-09-04
Distribution
AZ, CA, CO, CT, FL, GA, HI, IL, KS, KY, LA, MA, MD, ME, MO, NC, NE, NJ, NY, OH, OK, OR, PA, TX, UT, VA, WA, Costa Rica, Panama
Firm state
NY
Product quantity
477 cases total for all products
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Documentation & Change Control
Reason for recall

Products may contain undeclared sesame

Product description

Prime Food brand Steam Bun with Egg Custard & Coconut Added; 10pcs/pack; NET WT. 20 oz (1lb.4 oz) 568g; KEEP FROZEN; INGREDIENTS: Dough: Bleached Wheat Flour, Water, Sugar, Salad Oil (Soybean Oil, Canola Oil), Food Starch-Modified, Instant Yeast (Yeast (Saccharomyces Cerevisiae), Sorbitan Monostearate, Ascorbic Acid), Baking Powder (Corn Starch, Sodium Bicarbonate, Sodium Aluminum Sulfate, Monocalcium Phosphate). Filling: Evaporated Milk (Milk, Dipotassium Phosphate, Carrageenan, Vitamin D3), Sweetened Condensed Milk (Milk, Sugar), Cream of Coconut (Coconut, Sugar, Water, Polysorbate 60, Sorbitan Monostearate, Salt, Propylene Glycol Alginate, Mono and Diglycerides (Emulsifiers), Citric Acid, Guar Gum Locust Bean), Unsalted Butter (Cream, Natural Flavors), Sugar, Egg, Coconut Milk (Coconut Extract, Water, Citric Acid (as Antioxidant), Sodium Metabisulfite (as Preservative)), Desiccated Coconut (Coconut, Sulfite), Custard Powder (Corn Starch, Artificial & Natural Flavorings, FD&C Yellow #5 and #6, Salt, Flavour Enhancer), Bleached wheat Flour, Corn Strach, Egg Yellow Shade (Water, FD&C Yellow #5 and #6, Citric Acid, Caramel Color, Sodium Benzoate (Preservative)).; CONTAINS: WHEAT, SOY, MILK, EGG, COCONUT, SULFITE

Code / lot info

Lot # 24149 and Expiration Date October 2025 Lot # 24150 and Expiration Date October 2025

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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.