FDA recall record

Green Mountain Coffee Roasters Master Cases, Product Code #8534 recall — FDA F-1584-2013

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

Class IIclassification
F-1584-2013official record ID
Jul 31, 2013report date

Recall record at a glance

Official recordF-1584-2013
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmGreen Mountain Coffee Roasters
Report dateJul 31, 2013
Recall initiation dateMay 3, 2013
Quantity288,144 kcups/4,002 master cases (6 retail boxes per case)/ 24,012 retail boxes
LocationWaterbury, VT, United States

Official 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

Why the product was recalled

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

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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