Class IITerminated in FDA datasetRecall initiated May 3, 2013

Master Cases, Product Code #8534 (6-12 count retail boxes) Label of master case bears the name:…

Recalling firm: Green Mountain Coffee Roasters

Why it was recalled

Regular (caffeinated) Coffee individual K-cup packs were packaged inside multi unit retail boxes labeled Decaffeinated Coffee.

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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ProductMaster 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

FDA code information

Best By: 15NOV2013 PL113 3049

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Full FDA record and distribution details

Original product description

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

Original FDA recall reason

Regular (caffeinated) Coffee individual K-cup packs were packaged inside multi unit retail boxes labeled Decaffeinated Coffee.

Recall details

Recall number
F-1584-2013
Event ID
65057
FDA status
Terminated
Initiated
May 3, 2013
Reported
Jul 31, 2013
Classified
Jul 22, 2013
Terminated
Mar 24, 2016
Quantity
288,144 kcups/4,002 master cases (6 retail boxes per case)/ 24,012 retail boxes
Location
Waterbury, VT, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

TX, LA, MD, IN, IL, NE, NC, MN, WI, FL, AL

FDA source record · F-1584-2013

Data updated September 16, 2026. View official FDA data ↗

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