FDA Recall United States Terminated Historical recordClass II
Keurig Dr Pepper, Inc.
- Product
- Newman's Own Organics, Newman's Special Decaf Medium Roast,…
- Published
- September 9, 2020
- Distribution
- New York, Connecticut, Pennsylvania, Mai…
Keurig Dr Pepper, Inc. Recall: Product is labeled as decaf, but might contain caffeine.
United States
TerminatedClass II
- Company
- Keurig Dr Pepper, Inc.
- Product
- McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz…
- Recall date
- December 6, 2025
- Terminated
- May 21, 2026
- Source
- FDA
Reason for recall
Product is labeled as decaf, but might contain caffeine.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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. | 043000073438 | 960 cartons (84 pods/carton) | Best By 17 NOV 2026 LA hh:mm PL070 5321 or 5322 Batch Number: 5101564894 Material Number: 5000358463 ASIN: B07GCNDL91 |
Distribution
- CA
- IN
- NV
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0419-2026
- Event ID
- 98138
- Status
- Terminated
- Classification
- Class II
- Company
- Keurig Dr Pepper, Inc.
- Product description
- 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.
- Quantity
- 960 cartons (84 pods/carton)
- Reason
- Product is labeled as decaf, but might contain caffeine.
- Recall initiation date
- December 6, 2025
- Report date
- February 4, 2026
- Classification date
- Not published in this source record
- Termination date
- May 21, 2026
- Distribution pattern
- CA, IN, NV
- UPC, lot, and code information
- UPC 043000073438; Best By 17 NOV 2026 LA hh:mm PL070 5321 or 5322 Batch Number: 5101564894 Material Number: 5000358463 ASIN: B07GCNDL91
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Keurig Dr Pepper, Inc.
Other recalls from Keurig Dr Pepper, Inc.
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| California | 1 |
| Indiana | 1 |
| Nevada | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
