FDA recall record
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...
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of May 21, 2026. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
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.
Reason
Product is labeled as decaf, but might contain caffeine.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
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.
Code information listed by FDA
Best By 17 NOV 2026 LA hh:mm PL070 5321 or 5322 Batch Number: 5101564894 Material Number: 5000358463 ASIN: B07GCNDL91
Distribution and firm information
Recalling firm listed by FDA: Keurig DR Pepper, Inc.
Firm location listed by FDA: Knoxville, TN, United States
Distribution reported by FDA: CA, IN, NV
Product quantity listed by FDA: 960 cartons (84 pods/carton)
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.