Green Mountain Coffee Roasters
Green Mountain Coffee Roasters has 3 FDA enforcement events on this register (4 product records) between 2013 and 2014: 3 food; the busiest year was 2013 with 2.
0% of its events are Class I; the most common class is Class II (2). 0 events are listed as ongoing; the recalling firm's address is in VT.
Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.
Enforcement events
| Initiated | Product (first record) | Type | Class | Records | Status |
|---|---|---|---|---|---|
| 10 Jan 2014 | Newmans Own¿ Organics Newmans Special Blend 80 Count K-Cup¿ Packs; UPC 09955515593; Product Code: 15593 281792 | Food | Class II | 1 | Terminated |
| 6 Sep 2013 | Tullys¿ House Blend Coffee 12-ct K-Cup¿ packs; Product Code: 8802 (Case of 6 - 12 count retail boxes) UPC: 10099555088028 | Food | Class III | 2 | Terminated |
| 3 May 2013 | Master 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 Packs | Food | Class II | 1 | Terminated |
By type and class
Class I: 0% of this firm's events; 18% of all events on the register.
Events by year
Questions and answers
How many FDA recalls has Green Mountain Coffee Roasters had?
3 enforcement events (4 product records) on this register, 2013–2014: 3 food.
Are any Green Mountain Coffee Roasters recalls ongoing?
0 events are listed as ongoing in the current openFDA export.
What class are Green Mountain Coffee Roasters recalls?
2 Class II, 1 Class III. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.
Where does this data come from?
openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.
Provenance
Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.