Food recall

CinFranky LLC dba New Mexico Pinon Coffee recall: New Mexico Pinon Coffee

CinFranky LLC dba New Mexico Pinon Coffee, of Albuquerque, NM, recalled New Mexico Pinon Coffee. The FDA's reason: “Clear coat seal on the lid of the single serve cups did not get applied consistently to all cups in the production run. This resulted in the food safe ink printing on some cups to run when exposed...” The FDA classified it Class III: it is unlikely to cause harm. The company began the recall voluntarily on June 20, 2025, and the FDA first listed it in its Enforcement Report of July 23, 2025. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class III

It is unlikely to cause harm

Why

Other germs or toxins (botulism, hepatitis A, mold...)

Status

Terminated

Closed August 11, 2025

The recall

Company
CinFranky LLC dba New Mexico Pinon Coffee (Albuquerque, NM)
Reason, in FDA's words
“Clear coat seal on the lid of the single serve cups did not get applied consistently to all cups in the production run. This resulted in the food safe ink printing on some cups to run when exposed to high temperature, high-pressure water used in a K-cup machine.”
Where it was sold
Nationwide
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
97171

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-0273-2025 Class III

    New Mexico Pinon Coffee. Dark Pinon Single Serve 10ct. Product Number:F03308 UPC:812361033081. Single Serve (Keurig) Cups, filled with ground coffee flavored with natural flavorings.

    Codes: Lot Code: 251749 Best Buy Date: 05/08/2026

    Quantity: 154 Eaches

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of July 23, 2025.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.