CLASS II Food recall · Reported 5 Mar 2014 · FDA Enforcement Report
Newmans Own¿ Organics Newmans Special Blend K-Cup¿ Packs recalled
Green Mountain Coffee Roasters is recalling Newmans Own¿ Organics Newmans Special Blend K-Cup¿ Packs, distributed in Georgia, Tennessee. The recall was initiated on 10 Jan 2014 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1592-2014
- FDA event ID
- 67258
- Recalling firm
- Green Mountain Coffee Roasters, Waterbury, VT
- Brand
- Newmans Own
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 10 Jan 2014
- FDA classified
- 27 Feb 2014
- Reported
- 5 Mar 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Packaging Defects
- Product category
- Coffee
Timeline
| 10 Jan 2014 | Recall initiated by company | |
| 27 Feb 2014 | Classified by FDA | +48 days |
| 5 Mar 2014 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Some individual Coffee K-Cup¿ packs (caffeinated) received Decaffeinated lids/labels during packaging.
Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.
Product as listed by the FDA
Newmans Own¿ Organics Newmans Special Blend 80 Count K-Cup¿ Packs; UPC 09955515593; Product Code: 15593 281792
Where it was distributed
GA, TN
Questions about this recall
Why was it recalled?
Some individual Coffee K-Cup¿ packs (caffeinated) received Decaffeinated lids/labels during packaging.
Which lots are affected?
Lot Number: LA 15593 PL086 3300
Where was it sold?
GA, TN
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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