Recall record at a glance
| Official record | F-1750-2024 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Prime Food Processing Corp. |
| Report date | Sep 4, 2024 |
| Recall initiation date | Aug 9, 2024 |
| Quantity | 477 cases total for all products |
| Location | Brooklyn, NY, United States |
Official 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
Why the product was recalled
Products may contain undeclared sesame
Distribution information
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
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
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