Tullys¿ House Blend Coffee 12-ct K-Cup¿ packs; Product Code: 8802 (Case of 6 - 12 count retail…
Recalling firm: Green Mountain Coffee Roasters
Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 24, 2016.
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FDA code information
Best By: 27 MAR 2014, 28 MAR 2014 Lot Numbers: NA 8802 PL055 3181, NA 8802 PL055 3182
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Full FDA record and distribution details
Original product description
Tullys¿ House Blend Coffee 12-ct K-Cup¿ packs; Product Code: 8802 (Case of 6 - 12 count retail boxes) UPC: 10099555088028
Original FDA recall reason
Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes.
Recall details
- Recall number
- F-1965-2013
- Event ID
- 66131
- FDA status
- Terminated
- Initiated
- Sep 6, 2013
- Reported
- Oct 9, 2013
- Classified
- Sep 30, 2013
- Terminated
- Mar 24, 2016
- Quantity
- 4,697 master cases (6 retail boxes per case)
- Location
- Waterbury, VT, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
IL, CA, OR, WA, UT
Data updated September 16, 2026. View official FDA data ↗
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