Pingo Peanut Butter Cookie Hot Chocolate packaged in single serve pods. Pods are packaged in the following Pingo Variety Pack boxes: Pingo Hot Chocolate Pods Variety Pack, 40 ...
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What this record tells you
This FDA record concerns Pingo Peanut Butter Cookie Hot Chocolate packaged in single serve pods. Pods are packaged in the following Pingo Variety Pack boxes: Pingo Hot Chocolate Pods Variety Pack, 40 ... 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
Compare UPC/GTIN, lot or batch code, package size, flavor or variety, and any best-by/use-by date listed in the notice.
FDA public announcements can appear before an enforcement report is classified, so an empty classification does not mean the notice is unimportant.
Product Description & Identification
Pingo Peanut Butter Cookie Hot Chocolate packaged in single serve pods. Pods are packaged in the following Pingo Variety Pack boxes: Pingo Hot Chocolate Pods Variety Pack, 40 Count UPC: 810683028150 Pingo Hot Chocolate Pods Variety Pack, 100 Count UPC: 810683029805 Pingo Hot Chocolate Pods Peanut Butter Cookie, 100 Count UPC: 810683028754 Pingo Hot Chocolate Pods Peanut Butter Cookie, 40 Count UPC: 810683028037
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.
- Confirm the full product and brand or recalling-firm name.
- Compare package size, color, flavor, model, style, or configuration when listed.
- Check UPC, lot, batch, serial, date code, recall number, or USDA establishment number.
- Review the recall date and distribution information without assuming every seller is listed.
- 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
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.
Open FDA Source Record →Record Transparency
- Issuing agency
- FDA
- Source ID
- F-0582-2023
- Indexed update
- 2026-08-09 21:59:13 UTC
- Official source
- Open issuing-agency record