Food, drugs, devices › Green Mountain Coffee Roasters
Food recall: Master Cases, Product Code #8534 (6-12 count retail boxes) Label of master case bears the name: Donut House K -Cup Packs
Green Mountain Coffee Roasters (Waterbury, VT) initiated this food recall on 3 May 2013; FDA lists 1 product record under event 65057, classified Class II.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 52% of the 546 food enforcement events initiated in 2013 carry the same class.
Status: Terminated, terminated 24 Mar 2016. Initiation: voluntary: firm initiated. Green Mountain Coffee Roasters has 3 enforcement events on this register, with a median of 1 product record per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Green Mountain Coffee Roasters, Waterbury, VT.
Reason for recall
"Regular (caffeinated) Coffee individual K-cup packs were packaged inside multi unit retail boxes labeled Decaffeinated Coffee."
Distribution
"TX, LA, MD, IN, IL, NE, NC, MN, WI, FL, AL"
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1584-2013 | 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 | 288,144 kcups/4,002 master cases (6 retail boxes per case)/ 24,012 retail boxes | Class II | Terminated | 31 Jul 2013 |
Context
Other enforcement events for Green Mountain Coffee Roasters
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 10 Jan 2014 | Newmans Own¿ Organics Newmans Special Blend 80 Count K-Cup¿ Packs; UPC 09955515593; Product Code: 15593 281792 | Food | Class II | 1 |
| 6 Sep 2013 | Tullys¿ House Blend Coffee 12-ct K-Cup¿ packs; Product Code: 8802 (Case of 6 - 12 count retail boxes) UPC: 1009955508802 | Food | Class III | 2 |
All 3 events for Green Mountain Coffee Roasters
Questions and answers
Why was this food recalled?
FDA's record gives the reason for recall as: "Regular (caffeinated) Coffee individual K-cup packs were packaged inside multi unit retail boxes labeled Decaffeinated Coffee."
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "TX, LA, MD, IN, IL, NE, NC, MN, WI, FL, AL"
Is the recall still ongoing?
FDA lists the status as Terminated; the termination date is 24 Mar 2016. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.