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FDA source record Class III Terminated

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 Var...

Recall Date: 2023-01-31 Recalling Firm: TWO RIVERS COFFEE LLC Record Ref: F-0581-2023

FINDARECALL QUICK READ

What this record tells you

This FDA record concerns 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 Var... and names TWO RIVERS COFFEE LLC as the recalling firm. Use the source fields below to narrow the match, then verify the exact item and current remedy on the issuing-agency page.

  • Firm: TWO RIVERS COFFEE LLC
  • Classification: Class III
  • Status: Terminated
  • Recall date: 2023-01-31
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Product Description & Identification

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

Reason for Recall / Hazard Identified

Coffee pods may contain undeclared peanut residue

How to Check Whether Your Product Matches

A matching product name or photograph is not enough by itself. Compare every identifier available on your item or packaging with the official notice.

  1. Confirm the full product and brand or recalling-firm name.
  2. Compare package size, color, flavor, model, style, or configuration when listed.
  3. Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
  4. Review the recall date and distribution information without assuming every seller is listed.
  5. Open the official FDA source below and follow its current instructions.

If a required identifier is missing, contact the recalling company or issuing agency through the official notice rather than guessing.

Consumer Action Recorded in the Source

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Distribution & Affected States

Distributed to distributors in WI and WA and distributed nationwide to consumers.

Verify With the Issuing Agency

This record was last updated in our index on 2026-08-09 21:59:13 UTC. Because recall enforcement statuses and instructions evolve, always verify details directly with the issuing government agency.

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Record Transparency

Issuing agency
FDA
Source ID
F-0581-2023
Indexed update
2026-08-09 21:59:13 UTC
Official source
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