FDA recall record

Torn & Glasser Dark Chocolate Expresso Beans recall — FDA F-0458-2021

Dark Chocolate walnuts were packed in a container labeled at Dark Chocolate Espresso Beans and does not declare walnuts as an allergen Bottom label with…

Class IIclassification
F-0458-2021official record ID
May 5, 2021report date

Recall record at a glance

Official recordF-0458-2021
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmTorn & Glasser, Inc.
Report dateMay 5, 2021
Recall initiation dateApr 13, 2021
Quantity622 cases (7464 units)
LocationPomona, CA, United States

Official product description

Dark Chocolate Expresso Beans; Net Wt. 12 oz. (340g), Best if used by 11-19-2021. Contains Soy, May Contain Milk. Packed in a facility that processes on share equipment with Peanuts, Tree Nuts, Milk, Wheat and Egg. UPC: 0 72488 99868 1 Packed by Torn & Glasser, Los Angeles, CA

Why the product was recalled

Dark Chocolate walnuts were packed in a container labeled at Dark Chocolate Espresso Beans and does not declare walnuts as an allergen Bottom label with nutritional information is correct for the Dark Chocolate Walnuts.

Distribution information

Alaska, Alabama, Arizona, Arkansas, California, Georgia, Illinois, Indiana, Idaho, Kansas, Kentucky, Louisiana, Michigan, Mississippi, Missouri, Montana, Nebraska, Nevada, New Mexico, Ohio, Oregon, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin, Wyoming

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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