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    Product: Caramel macchiato

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    anonymous11178
    Just looking at that is making me nauseous again.
    Reply 6 days ago
    Jumbo has issued a recall of their Liver cheese due to the presence of Listeria Monocytogenes. The product was sold by Jumbo Supermarkets in the Netherlands.

    The affected product is Jumbo Liver cheese with an EAN code of 8718452611065 and a best-before date of 02/11/2023.

    If you... See More have the recalled products in your home, please do not eat them, throw them away or return them to the place of purchase.

    In case you are experiencing Listeria monocytogenes symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain, and diarrhea, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

    Source: nvwa.nl
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    Daiso California LLC of La Mirada, CA is recalling the below listed Tohato and Kashiwado snacks due to undeclared allergen ingredients. People who have an allergy or severe sensitivity to almonds, peanuts, soybeans, milk, and shellfish run the risk of serious or life-threatening allergic reaction if they... See More consume these products. Tohato and Kashiwado Snacks were sold in Daiso stores in California, Washington, Nevada, Texas, New York, and New Jersey. There have been no reported cases of allergic reaction to these products.

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    SKU: 4901940039432, Product Name: TOHATO Caramel Corn - Boys Festival 80g, Missing Allergen: Almond Peanut
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    In case you experienced harm from allergens or undeclared ingredients, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

    Company name: Daiso California, LLC
    Brand name: TOHATO and KASHIWADO
    Product recalled: Popcorn and other snacks
    Reason of the recall: Undeclared almonds, peanuts, soybeans, milk, and shellfish
    FDA Recall date: January 10, 2023

    Source: fda.gov
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