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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 98138

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
December 06, 2025
Product types
Food
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Keurig DR Pepper, Inc.

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

1 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 1

McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g), packaged as an 84-count carton, UPC 043000073438. Distributed By: Keurig Green Mountain, Inc. Burlington, MA 01803 U.S.A.

H-0419-2026
Recall number
H-0419-2026
Initiated
December 06, 2025
Classification
Class II
Status
Terminated
Recalling firm
Keurig DR Pepper, Inc.
Quantity
960 cartons (84 pods/carton)

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Product is labeled as decaf, but might contain caffeine.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Product is labeled as decaf, but might contain caffeine.

Code information

Best By 17 NOV 2026 LA hh:mm PL070 5321 or 5322 Batch Number: 5101564894 Material Number: 5000358463 ASIN: B07GCNDL91

Distribution pattern

CA, IN, NV