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Keurig DR Pepper, Inc. recall - McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g),…
FDA (enforcement) · February 4, 2026 · Class II
- Keurig DR Pepper, Inc. recalled McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g), packaged as an… - an FDA enforcement event posted , classified Class II, covering 1 product entry.
- FDA-stated reason: Product is labeled as decaf, but might contain caffeine.
- Details as of ; the linked official notice is authoritative for lot codes, VINs, and remedies.
- Agency
- FDA
- Posted
- Initiated
- Classification
- Class II
- Status
- Terminated
- Recalling firm
- Keurig DR Pepper, Inc.
- Source ID
- 98138
FDA Enforcement Report search →
How this recall compares
- Keurig DR Pepper, Inc has 6 recall events in the FDA (2012+) and USDA-FSIS (2014+) records tracked here; by posting date this is the 6th. The one before it: KEURIG DR PEPPER recall - Celestial Seasonings Mandarin Orange Spice Herbal Tea… ().
Other recalls from Keurig DR Pepper, Inc
| Posted | Agency | Recall | Class |
|---|---|---|---|
| FDA | KEURIG DR PEPPER recall - Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup… | Class II | |
| FDA | KEURIG DR PEPPER recall - Diet Snapple Tea Peach Tea 16 oz. packaged in PET bottle.… | Class II | |
| FDA | KEURIG DR PEPPER recall - Target Good & Gather Coconut Pineapple Sparkling Water 8 pack… | Class II | |
| FDA | KEURIG DR PEPPER recall - Rc Cola 12 Oz (355 mL) packaged in an aluminum can 12 can to a… | Class II | |
| FDA | Keurig Dr Pepper, Inc. recall - Newman's Own Organics, Newman's Special Decaf Medium… | Class II |
Matched by company name after removing suffixes such as Inc. and LLC; parent companies and subsidiaries are counted separately.
Product entries (1)
| Recall # | Product | Codes / lots | Distribution |
|---|---|---|---|
| H-0419-2026 | 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,… | Best By 17 NOV 2026 LA hh:mm PL070 5321 or 5322 Batch Number: 5101564894 Material… | CA, IN, NV |
FDA enforcement entries have no per-recall public URL - verify via the FDA Enforcement Report search using the firm name or a recall number above.
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