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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 66131

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
September 06, 2013
Product types
Food
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Green Mountain Coffee Roasters

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 2

Tullys¿ House Blend Coffee 12-ct K-Cup¿ packs; Product Code: 8802 (Case of 6 - 12 count retail boxes) UPC: 10099555088028

F-1965-2013
Recall number
F-1965-2013
Initiated
September 06, 2013
Classification
Class III
Status
Terminated
Quantity
4,697 master cases (6 retail boxes per case)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Best By: 27 MAR 2014, 28 MAR 2014 Lot Numbers: NA 8802 PL055 3181, NA 8802 PL055 3182

Distribution pattern

IL, CA, OR, WA, UT

food · product 2 of 2

Tully's House Blend Decaffeinated K-Cup¿ Packs (12-ct retail box) Product Code: 8803; UPC: 099555088038

F-1966-2013
Recall number
F-1966-2013
Initiated
September 06, 2013
Classification
Class III
Status
Terminated
Quantity
28,182 retail boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Individual regular (caffeinated) K-Cup packs were packaged inside multiunit Decaffeinated retail boxes.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Best By: 27 MAR 2014, 28 MAR 2014 Lot Numbers: NA PL055 3181, NA PL055 3182

Distribution pattern

IL, CA, OR, WA, UT