FDA recall record
Tullys¿ House Blend Coffee 12-ct K-Cup¿ packs; Product Code: 8802 (Case of 6 - 12 count retail boxes) UPC: 10099555088028
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of March 24, 2016. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Tullys¿ House Blend Coffee 12-ct K-Cup¿ packs; Product Code: 8802 (Case of 6 - 12 count retail boxes) UPC: 10099555088028
Reason
Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Tullys¿ House Blend Coffee 12-ct K-Cup¿ packs; Product Code: 8802 (Case of 6 - 12 count retail boxes) UPC: 10099555088028
Code information listed by FDA
Best By: 27 MAR 2014, 28 MAR 2014 Lot Numbers: NA 8802 PL055 3181, NA 8802 PL055 3182
Distribution and firm information
Recalling firm listed by FDA: Green Mountain Coffee Roasters
Firm location listed by FDA: Waterbury, VT, United States
Distribution reported by FDA: IL, CA, OR, WA, UT
Product quantity listed by FDA: 4,697 master cases (6 retail boxes per case)
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.