Newmans Own¿ Organics Newmans Special Blend 80 Count K-Cup¿ Packs; UPC 09955515593…
Green Mountain Coffee Roasters recalled this product and the FDA reported the enforcement action on 5 March 2014 as Class II. The recall was initiated by the firm. Some individual Coffee K-Cup¿ packs (caffeinated) received Decaffeinated lids/labels during packaging.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Newmans Own¿ Organics Newmans Special Blend 80 Count K-Cup¿ Packs; UPC 09955515593; Product Code: 15593 281792
- UPC
- 09955515593
- Reason for recall
- Some individual Coffee K-Cup¿ packs (caffeinated) received Decaffeinated lids/labels during packaging.
- Recalling firm
- Green Mountain Coffee Roasters
- Firm location
- Waterbury, Vermont, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-1592-2014
- Quantity
- 8,928 retail boxes
- Distribution
- GA, TN
- Initiated
- 10 January 2014
- Reported by FDA
- 5 March 2014
- Terminated
- 9 March 2016
- Firm notified by
- Product codes
- Lot Number: LA 15593 PL086 3300
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This record is the only one the FDA opened for its recall event, so it covers a single product code.
- The recall ran for 2.2 years, from 10 January 2014 to termination on 9 March 2016. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 2 states, and the FDA published the enforcement report 8 weeks after the firm began the recall.
- The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.
Named in the distribution pattern: Georgia, Tennessee. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
Other records from Green Mountain Coffee Roasters
The FDA opens one enforcement record per product code, so several of these are frequently one recall event.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2013-10-09 | Tully's House Blend Decaffeinated K-Cup¿ Packs (12-ct retail box) Product Code: 8803; UPC: 099555088038 | Green Mountain Coffee Roasters | Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes. | Class III |
| 2013-10-09 | Tullys¿ House Blend Coffee 12-ct K-Cup¿ packs; Product Code: 8802 (Case of 6 - 12 count retail boxes) UPC: 10099555088028 | Green Mountain Coffee Roasters | Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes. | Class III |
| 2013-07-31 | 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 | Green Mountain Coffee Roasters | Regular (caffeinated) Coffee individual K-cup packs were packaged inside multi unit retail boxes labeled Decaffeinated Coffee. | Class II |
All 4 records for Green Mountain Coffee Roasters
All 2014 recalls · All FDA food recall data
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.