Skip to content
Food Recall Radar
Class IIFDAF-0021-2020

STARK INC. recalls Ritter Sport KAFFEESPLITTER Chocolate with caramelized coffee beans; Net Weight: 3.5oz / 1 (Class II)

Ritter Sport recalled Kaffeesplitter chocolate with caramelized coffee beans because the product contains undeclared milk. Consumers with milk allergies could experience allergic reactions.

Class IIEating this product may cause temporary or medically reversible health problems; serious harm is unlikely.

Product

Ritter Sport KAFFEESPLITTER Chocolate with caramelized coffee beans; Net Weight: 3.5oz / 100g; Ingredients: sugar, cocoa mass, caramelized pieces of coffee beans (sugar, coffee (roasted) (4%), sunflower oil), cocoa butter, butter pure fat, emulsifier: lecithin (soy) May contain traces of peanuts, nuts, and egg. Manufactured by Alfred Ritter GmbH & Co. KG D-71111 Waldenbuch, Deutschland Product of Germany UPC: 000417 927002

Reason for recall

Product contains undeclared milk.

Affected products (1)

Recall #ProductLot / codeStatus
F-0021-2020Ritter Sport KAFFEESPLITTER Chocolate with caramelized coffee beans; Net Weight: 3.5oz / 100g; Ingredients: sugar, cocoa mass, caramelized pieces of coffee beans (sugar, coffee (roasted) (4%), sunflower oil), cocoa butter, butter pure fat, emulsifier: lecithin (soy) May contain traces of peanuts, nuts, and egg. Manufactured by Alfred Ritter GmbH & Co. KG D-71111 Waldenbuch, Deutschland Product of Germany UPC: 000417 927002All codes.Terminated

Related recalls

Likely Class I(our estimate, pending agency classification)FDA

Made Fresh Salads Inc. recalls Made Fresh Salads Ready to Eat Deli Style Salads and cream cheese

Made Fresh Salads recalled ready-to-eat deli style salads and cream cheese due to potential Listeria monocytogenes contamination. Listeria infection can cause severe illness and is particularly dangerous for pregnant women, young children, and immunocompromised individuals.

Foreign materialListeriaBrand: Made Fresh Salads, Northside
Likely Class II(our estimate, pending agency classification)FDA

American Regent, Inc. recalls American Regent Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

American Regent recalled Epinephrine Injection USP 30 mg/30 mL multi-dose vials due to potential particulate matter and loss of sterility assurance. Users of affected vials face serious risk if the contamination is present, as injection of particles or non-sterile product could cause infection or other harm.

Foreign materialBrand: American Regent

Do not rely on this site to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Always check the original FDA or USDA notice, linked on every recall page.