FDA recall record

groundwork MIND-FULL Bar recall — FDA F-1016-2022

Oregon Department of Agriculture found that allergens were not properly declared during inspection.

Class Iclassification
F-1016-2022official record ID
May 4, 2022report date

Recall record at a glance

Official recordF-1016-2022
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmGroundwork Coffee LLC
Report dateMay 4, 2022
Recall initiation dateMar 28, 2022
LocationNorth Hollywood, CA, United States

Official product description

groundwork MIND-FULL Bar. Ingredients: Gluten-free oats, Flax seed, Chocolate chips, Brown sugar, Chia seeds, peanut butter, salt, cinnamon, coconut oil, agave, vanilla. Vegan, Gluten Free. Contains Nuts 671 Rose Ave. Venice, CA 90291

Why the product was recalled

Oregon Department of Agriculture found that allergens were not properly declared during inspection.

Distribution information

CA, OR

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

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.