Food Recall Check
Class II · Moderate risk Terminated Initiated Feb 27, 2021 (6 years ago)

B&G Sweet Heat Pepper Dip recall

Recalled by B&G Sweet Heat Peppers · Mead, WA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Cream Cheese and Sour Cream are declared, but milk is not declared on label.

Undeclared allergen: Milk

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

B&G Sweet Heat Pepper Dip, Ready To Eat, Refrigerated, packaged in 10 oz, semi-rigid plastic container. UPC 7 42832 07566 4. Product label is read in parts: "***SWEET HEAT PEPPER DIP ***Ingredients: Cream Cheese, Sour Cream, Jalapenos, Sugar, Apple Cider Vinegar, Granulated Garlic, Cayenne Pepper, Turmeric, Celery Seed ***KEEP REFRIGERATED ***BGSweetHeat.com ***Mead, WA 99021 ***".

Quantity: 43 cases (12/10 oz. containers per case)

Food: Spices & seasonings Sauces, dips & dressings Salads, sandwiches & prepared foods

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.

Best By: 3/5/2021 and 4/1/2021. Codes: 3 21037 and 3 21054

Where it was sold

Idaho Washington

FDA's distribution note: distributed in ID and WA.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to milk; 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
B&G Sweet Heat Peppers
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 27, 2021
In FDA report of
Apr 14, 2021
Terminated
Apr 14, 2021
FDA recall number
F-0388-2021 · event 87477
Official record
FDA enforcement report search

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