Chocolate Ice Cream
Reason During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products. The products also lacked the…
Recalled by Koogee-Queen Anne, LLC · Louisville, KY, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products. The products also lacked the declaration that they are packaged in a facility that processes peanuts, tree nuts, wheat, milk and eggs.
Undeclared allergens: Milk Egg Peanut Tree nuts Wheat
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.
Java Chip Ice Cream, Manufactured by: Koogee-Queen Anne, LLC, d/b/a The Comfy Cow 2221 Frankfort Ave, Louisville, KY 40206.
Quantity: 1 - 3gal unit
Food: Ice cream Chips & snacks
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Codes on the products distributed to Comfy Cow retail locations are not tracked.
Indiana Kentucky
FDA's distribution note: Distributed in the states of Indiana and Kentucky
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, egg, peanut, tree nuts, wheat; 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.
FDA files each product of one recall action separately; these share the same FDA event.
Reason During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products. The products also lacked the…
Reason During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products. The products also lacked the…
Reason During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products. The products also lacked the…
Reason During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products. The products also lacked the…
Reason During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products. The products also lacked the…
Reason During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products. The products also lacked the…
Reason During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products. The products also lacked the…
Reason During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products. The products also lacked the…
Reason During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products. The products also lacked the…
Reason During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products. The products also lacked the…
Reason During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products. The products also lacked the…
Reason During an FDA inspection the firm was notified that their bulk product lacked labels. Due to the lack of ingredient statement, the firm failed to declare direct allergens for the products. The products also lacked the…
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Reason The firm is recalling various brands of ice cream due to E. coli & high Coliform Bacteria counts in various products.
Reason The firm is recalling various brands of ice cream due to E. coli & high Coliform Bacteria counts in various products.
Reason The firm is recalling various brands of ice cream due to E. coli & high Coliform Bacteria counts in various products.
Reason The firm is recalling various brands of ice cream due to E. coli & high Coliform Bacteria counts in various products.