FDA recall record

Lidl US Operations Vemondo Vegan Coconut & Cocoa Non-Dairy Dessert Cones 4-3.7 fl recall — FDA F-0394-2022

Undeclared milk allergen

Class IIclassification
F-0394-2022official record ID
Jan 19, 2022report date

Recall record at a glance

Official recordF-0394-2022
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmLidl US Operations, LLC
Report dateJan 19, 2022
Recall initiation dateDec 10, 2021
Quantity729 units (total)
LocationFredericksburg, VA, United States

Official product description

Vemondo Vegan Coconut & Cocoa Non-Dairy Dessert Cones 4-3.7 fl ounces (110 mL) cones UPC 4 056489 468646

Why the product was recalled

Undeclared milk allergen

Distribution information

Distributed to retail stores in MD, VA, and PA.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.