Recall record at a glance
| Official record | F-0581-2023 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Terminated |
| Recalling firm | TWO RIVERS COFFEE LLC |
| Report date | Mar 22, 2023 |
| Recall initiation date | Jan 31, 2023 |
| Quantity | Approximately 90,000 cups total |
| Location | South Plainfield, NJ, United States |
Official product description
Brooklyn Bean Peanut Butter Cup Hot Cocoa packaged in single serve pods. Pods are packaged in the following Brooklyn Beans Variety Pack boxes: Brooklyn Beans Hot Chocolate Variety Pack Pods, 12 Count UPC:810683021977 Brooklyn Beans Brooklyn Beans Peanut Butter Chocolate Hot Cocoa Pods, 40 Count UPC: 810683023018 Brooklyn Beans Hot Chocolate Variety Pack Pods, 40 Count UPC:810683022974
Why the product was recalled
Coffee pods may contain undeclared peanut residue
Distribution information
Distributed to distributors in WI and WA and distributed nationwide to consumers.
How to read the classification
FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Press Release.
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.