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RECALL RECORD — CLASS IIIRecall closedF-1966-2013/FDA enforcement
Green Mountain Coffee Roasters·Food·Sep 6, 2013

Tully's House Blend Decaffeinated K-cup¿ Packs (12-ct Retail Box) Product Code: 8803

What you need to know

Class III

  • What happened

    Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDAIL, CA, OR, WA +1 moreMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameGreen Mountain Coffee Roasters
Recalling firmGreen Mountain Coffee RoastersWaterbury, VT, United States
UPC / barcodes
0 99555 08803 8
Lot / date codes
  • Best By: 27 MAR 2014, 28 MAR 2014 Lot Numbers: NA PL055 3181, NA PL055 3182
Distribution area
ILCAORWAUT

IL, CA, OR, WA, UT

United States

Quantity affected28, 182 retail boxes
Recall initiationFDA report date: October 9, 2013
FDA recall numberF-1966-2013

Beyond the headline

The recall, in context

Green Mountain Coffee Roasters initiated this food recall on September 6, 2013. The FDA enforcement report states: Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes. The FDA report lists distribution as: IL, CA, OR, WA, UT.

The FDA enforcement report describes the reason as: Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes.

Tully's House Blend Decaffeinated K-cup¿ Packs (12-ct Retail Box) Product Code: 8803 was made or distributed by Green Mountain Coffee Roasters in Waterbury, VT, United States. This page reflects FDA report F-1966-2013, dated October 9, 2013.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Tully's House Blend Decaffeinated K-cup¿ Packs (12-ct Retail Box) Product Code: 8803 recall?

Green Mountain Coffee Roasters recalled Tully's House Blend Decaffeinated K-cup¿ Packs (12-ct Retail Box) Product Code: 8803 in an FDA Class III enforcement action reported as F-1966-2013. Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Green Mountain Coffee Roasters recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1966-2013. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Green Mountain Coffee Roasters

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Green Mountain Coffee Roasters

Tullys¿ House Blend Coffee 12-ct K-cup¿ Packs

Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes.

IL, CA, OR +2 moreFood

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.