FDA recall record

Sweet Earth Foods Aloha BBQ Quesadilla recall — FDA F-1834-2018

Firm received complaints of Sweet Earth Aloha BBQ Quesadilla packages that contain Mile High Quesadillas. Ingredient statement on outer package does not…

Class Iclassification
F-1834-2018official record ID
Aug 15, 2018report date

Recall record at a glance

Official recordF-1834-2018
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmSweet Earth Inc.
Report dateAug 15, 2018
Recall initiation dateAug 1, 2018
Quantity2453 casaes
LocationMoss Landing, CA, United States

Official product description

Sweet Earth Foods Aloha BBQ Quesadilla; 2 pack, NET WT 8 oz. Vegan: Pinto Beans, Red Onions, Pineapple and jalapenos with our vegan BBQ grounds and a cheddar-style vegan cheese. Keep Frozen. Ingredients: Filling: Vegan BBQ savory grounds (water, vital wheat gluten, onion, soy sauce, (water, soybeans, wheat, salt, alcohol), tomato paste, molasses, apple cider vinegar, canola oil, brown rice syrup, spices, nutritional yeast, garlic powder, bell pepper, ginger, natural hickory smoke, rice bran oil, rice vinegar, oregano, pinto beans (water, pinto beans), vegan cheddar style cheese (filtered water, coconut oil, modified food starch, {potato and corn], potato starch, sea salt, vegan cheddar flavor, olive oil extract, beta carotene, vitamin B12, red onion, pineapple (pineapple, pineapple juice and citric acid) Canola oil, jalapeno pepper, spices. WRAP: Water, unbleached white flour, canola oil, sea salt, baking powder (sodium bicarbonate, sodium acid pyrophosphate, potato starch) yeast, citric acid. Contains Soy, Wheat Manufactured in a facility that process egg, milk tree nuts. UPC: 016741000551 Sweet Earth Foods Moss Landing, CA 95039

Why the product was recalled

Firm received complaints of Sweet Earth Aloha BBQ Quesadilla packages that contain Mile High Quesadillas. Ingredient statement on outer package does not declare eggs or milk.

Distribution information

DC's in TX, CA, IL, IA, FL, MD

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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