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Coffee bean products

Beans / September 11, 2017

WARREN, Mich. - Lipari Foods, LLC has issued a voluntary recall of dark chocolate covered coffee beans packaged by sister company JLM due to an undeclared allergen of tree nuts (almonds). People who have an allergy or severe sensitivity to almonds run the risk of a serious or life-threatening allergic reaction if they consume these products. The products are safe for consumption by those who do not have an allergy or severe sensitivity to almonds.

The products were distributed to retail stores throughout Indiana, Kentucky, Michigan, Ohio, Pennsylvania, Tennessee, Wisconsin and West Virginia.

Products were distributed under the following brand names Angeli Foods, Harding's Markets, Goosberries Fresh Food Market, Martha's Vineyard, Hollywood Market, Daniels Foods, Snook's Butcher Shoppe, Martin's, Holiday Market, The Purple Onion, Remke Market or as generic product without branding.

The affected products can be identified by:

Product Lipari Product # Lot # Weight Best By Date UPC
Dark Chocolate Covered Coffee Beans (Angeli Foods, Harding's Markets, Goosberries Fresh Food Market, Martha's Vineyard, Hollywood Market, Daniels Foods, Snook's Butcher Shoppe, Martin's, Holiday Market, The Purple Onion, Remke Market)
Dark Chocolate Covered Coffee Beans (Generic)

There are no reported illnesses in connection with these products to date.

This was brought to our attention by our sister company, JLM who discovered that dark chocolate almonds were unintentionally mixed in with the dark chocolate covered coffee beans during packaging of private label products. As a precaution, Lipari Foods private label and non-branded products are being recalled as they have the potential to be contaminated. We are working closely with the FDA to ensure that all affected product has been pulled from commerce.

Consumers who have purchased this recalled product should not consume it. They should return it to the point of purchase. Consumers with questions should call Customer Service at 800-729-3354, 8:15 am - 4:30 pm, EST, Monday through Friday.

Source: www.fda.gov

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