FDA recall record
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 Hous...
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
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
Reason
Regular (caffeinated) Coffee individual K-cup packs were packaged inside multi unit retail boxes labeled Decaffeinated Coffee.
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.
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
Code information listed by FDA
Best By: 15NOV2013 PL113 3049
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: TX, LA, MD, IN, IL, NE, NC, MN, WI, FL, AL
Product quantity listed by FDA: 288,144 kcups/4,002 master cases (6 retail boxes per case)/ 24,012 retail boxes
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.