Class IITerminated in FDA datasetRecall initiated Sep 10, 2019

Ritter Sport KAFFEESPLITTER Chocolate with caramelized coffee beans; Net Weight: 3.5oz / 100g

Recalling firm: STARK INC.

Why it was recalled

Product contains undeclared milk.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 28, 2020.

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Compare the exact product and package details with the label you have.

ProductRitter 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
Package size3.5oz

FDA code information

All codes.

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Full FDA record and distribution details

Original product description

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

Original FDA recall reason

Product contains undeclared milk.

Recall details

Recall number
F-0021-2020
Event ID
83784
FDA status
Terminated
Initiated
Sep 10, 2019
Reported
Oct 16, 2019
Classified
Oct 7, 2019
Terminated
May 28, 2020
Quantity
189 cases; 24 pieces/case; total: 4,536 pieces
Location
Greenvale, NY, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

Products were distributed in: NY, OH, CA, WA, AZ, KS, WI, GA, NJ, MI, PA, UT, ID, MA, IL, CO, AL, SC, FL, VA, MN, MO, IN, TX, NV, LA, ME, OK

FDA source record · F-0021-2020

Data updated September 16, 2026. View official FDA data ↗

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