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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food
Food & Beverages/Beverages

McCafe Premium Roast Decaf Coffee K-Cups Recalled for Caffeine Presence

Agency Publication Date: January 23, 2026
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Summary

Keurig Dr Pepper, Inc. has voluntarily recalled 960 cartons of McCafe Premium Roast Decaf Coffee K-Cup Pods because the product may contain caffeine despite being labeled as decaffeinated. This recall involves the 84-count cartons distributed in California, Indiana, and Nevada. Consumers who purchased this specific batch should not consume the product if they must avoid caffeine for health or personal reasons.

Risk

The product may contain caffeine, which poses a risk to individuals with caffeine sensitivities or medical conditions that require a caffeine-free diet. Consuming unexpected caffeine can lead to symptoms such as rapid heart rate, insomnia, or elevated blood pressure.

What You Should Do

  1. Check your pantry for McCafe Premium Roast Decaf Coffee K-Cup Pods in 84-count cartons with UPC 043000073438.
  2. Verify if your package has the 'Best By' date of 17 NOV 2026 and Batch Number 5101564894 printed on the carton.
  3. Return the product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: McCafe Premium Roast Decaf Coffee K-Cup Pods (29 oz / 84-count)by McCafe
Item Code:
5000358463
UPC Codes:
043000073438
Lot Numbers:
5101564894
GTIN:
043000073438
Date Ranges: Best By 17 NOV 2026

ASIN: B07GCNDL91; Additional label codes: LA hh:mm PL070 5321 or 5322; Material Number: 5000358463.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98138
Status: Active
Manufacturer: Keurig DR Pepper, Inc.
Manufactured In: United States
Units Affected: 960 cartons (84 pods/carton)
Distributed To: California, Indiana, Nevada

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.