Food recall: Tullys House Blend Coffee 12-ct K-Cup packs; Product Code: 8802 (Case of 6 - 12 count retail boxes) UPC: 10099555088028
Class III FDA enforcement event 66131. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes.
Class III, in the words of FDA
a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences
Green Mountain Coffee Roasters started this food recall on 6 Sep 2013. The firm address in the FDA record is in Waterbury, VT. FDA put the recall in Class III. FDA event 66131 has 2 product records. The first FDA enforcement report date is 9 Oct 2013. The record gives the status Terminated, with the termination date 24 Mar 2016.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
IL, CA, OR, WA, UT
Recalling firm
Green Mountain Coffee Roasters, Waterbury, VT.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
2 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1965-2013 | Tullys House Blend Coffee 12-ct K-Cup packs; Product Code: 8802 (Case of 6 - 12 count retail boxes) UPC: 10099555088028 | 4,697 master cases (6 retail boxes per case) | Class III | Terminated | 9 Oct 2013 |
| F-1966-2013 | Tully's House Blend Decaffeinated K-Cup Packs (12-ct retail box) Product Code: 8803; UPC: 099555088038 | 28,182 retail boxes | Class III | Terminated | 9 Oct 2013 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class III: The lowest of the three FDA recall classes.
The event in context
- Food events that started in 2013
- 546
- Share of these events in Class III
- 11%
- Product records in this event
- 2Median of the firm: 1
- Events of the firm on the register
- 3
Other events of the firm
| 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 |
| 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 | Food | Class II | 1 |
Official channels
- FDA enforcement report F-1965-2013The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
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Cite this page
Recall Register. FDA enforcement event 66131. https://recallregister.com/fda/iii/66131/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
IL, CA, OR, WA, UT
- What quantity of product is in FDA event 66131?
- The event has 2 product records. The first record gives this quantity:
4,697 master cases (6 retail boxes per case)
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2013 have the same class?
- 11% of the 546 food events that started in 2013 are in Class III.