Green Mountain Coffee Roasters FDA recall records

The FDA has published 4 food recall enforcement records naming Green Mountain Coffee Roasters between 2013 and 2014, covering 3 separate recall events. The firm is recorded in Vermont. Data last updated 2 September 2026.

Records of 29,386
4
Share of all recalls
0%
Class I of 4
0
Reported between
2013 to 2014

What these records are

Every record on this page was published by the FDA in the openFDA food enforcement database. 4 records cover 3 recall events, because the agency opens one record per product code: a single recall of a product line with many codes appears here many times.

0 of these records are Class I, 2 Class II and 2 Class III. A recall count is not a safety score. Most FDA food recalls are initiated by the firm itself, and a recall is the firm removing product from the market, which is what a food safety plan is built to produce.

By year

Counts are by the date the FDA reported the enforcement action. That date runs behind the date a firm started a recall, so the most recent year is always partial.

Where the recalling firms are

The state is the location of the recalling firm, not where the product was sold. Distribution is recorded separately on each record.

Most recently reported

All 4 records.
ReportedProductFirmReasonClass
2014-03-05Newmans Own¿ Organics Newmans Special Blend 80 Count K-Cup¿ Packs; UPC 09955515593; Product Code: 15593 281792Green Mountain Coffee RoastersSome individual Coffee K-Cup¿ packs (caffeinated) received Decaffeinated lids/labels during packaging.Class II
2013-10-09Tully's House Blend Decaffeinated K-Cup¿ Packs (12-ct retail box) Product Code: 8803; UPC: 099555088038Green Mountain Coffee RoastersIndividual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes.Class III
2013-10-09Tullys¿ House Blend Coffee 12-ct K-Cup¿ packs; Product Code: 8802 (Case of 6 - 12 count retail boxes) UPC: 10099555088028Green Mountain Coffee RoastersIndividual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes.Class III
2013-07-31Master Cases, Product Code #8534 (6-12 count retail boxes) Label of master case bears the name: Donut House K -Cup Packs. 12-Count Retail Boxes, Product Code #8934, Donut House Decaffeinated K-Cup PacksGreen Mountain Coffee RoastersRegular (caffeinated) Coffee individual K-cup packs were packaged inside multi unit retail boxes labeled Decaffeinated Coffee.Class II

Questions

How many FDA recalls has Green Mountain Coffee Roasters had?
The FDA has published 4 food recall enforcement records naming Green Mountain Coffee Roasters between 2013 and 2014. Those records cover 3 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.
Does a high recall count mean a firm is unsafe?
Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.

All FDA food recall data

A recall is the end of an evidence trail that either existed or did not. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.