Keurig Recalls K-Cup Pods Due to Potential Contamination

New Mexico Piñon Coffee Recalls Dark Roast K-Cups Due to Potential Leaks

New Mexico Piñon coffee is initiating a recall of its single-serving Dark Piñon Single serve K-Cups. this action follows a report from the U.S. Food and Drug Administration (FDA) detailing potential issues with the product’s sealing.

The affected coffee was sold nationwide. The manufacturing process may have resulted in lids that where not properly sealed.This could lead to food-safe ink leaking into the coffee during the brewing process.

Understanding the Recall

This recall is classified as Class III, indicating a low risk of adverse health effects. The company has stated that no illnesses or injuries have been reported in connection with this recall.

The specific product involved is one lot of 10-count boxes featuring the lot code “251749.” Consumers should verify their packaging, as no other New Mexico Piñon Coffee products are part of this recall.

Consumer Guidance

Customers who purchased the affected K-Cups are advised to dispose of them or return them to the point of purchase for a refund. These steps ensure consumer safety and efficient product management.

For further data or assistance,customers can contact New Mexico Piñon Coffee directly at 505-298-1964. Proactive communication is key during product recalls.

Frequently Asked Questions

What is being recalled?

New Mexico Piñon Coffee Dark Piñon Single Serve K-Cups, lot code “251749.”

Why is it being recalled?

Potential for lids to be improperly sealed, which could lead to ink leaking into the coffee.

Is this a serious health risk?

No, it is indeed a Class III recall, meaning it is unlikely to cause negative health effects.

What should I do if I have the recalled product?

Dispose of the product or return it to the place of purchase for a refund.

Who can I contact for more information?

New Mexico Piñon Coffee at 505-298-1964.

Have you encountered this issue with your coffee? Share your experience or thoughts in the comments below, and let others know.

What are the specific symptoms of a Listeria monocytogenes infection (listeriosis)?

Understanding the recent Keurig K-Cup Recall

Keurig Dr Pepper has issued a voluntary recall of certain K-Cup pods due to potential contamination with listeria monocytogenes. This recall impacts a specific batch code range and affects several popular Keurig coffee brands. Understanding the details of this K-Cup recall is crucial for consumers who use Keurig coffee makers and rely on the convenience of single-serve coffee.

What K-Cup Pods Are Affected?

The recall specifically targets K-Cup pods manufactured before June 18, 2025, with the following characteristics:

Brands Affected: Includes Keurig, Van Houtte, and Café Du Monde K-Cup pods.

Batch Codes: Look for batch codes beginning with “X” followed by a series of numbers. A complete list of affected batch codes is available on the Keurig website (link to official recall page should be inserted here).

UPC Codes: specific UPC codes are also identified in the recall notice. Refer to the official keurig recall proclamation for a extensive list.

Distribution: These pods were sold nationwide in the United States and Canada through various retailers,including major grocery stores,club stores,and online platforms.

The Risk of Listeria monocytogenes

Listeria monocytogenes is a bacterium that can cause a serious infection called listeriosis. Symptoms can include:

Fever

Muscle aches

Headache

Stiff neck

Confusion

Loss of balance

Convulsions

Listeriosis is particularly dangerous for:

Pregnant women

Newborns

Older adults

people with weakened immune systems

How to identify Recalled K-Cup Pods

Identifying potentially contaminated K-Cup pods requires careful inspection of the packaging.

1. locate the Batch Code: The batch code is typically printed on the top of the K-Cup pod box.
2. Compare to Recall List: Cross-reference the batch code with the list provided by Keurig on their official recall webpage.
3. Check UPC Codes: verify the UPC code on your packaging against the recalled UPC list.
4. If Uncertain, Contact keurig: If you are unsure whether your K-Cup pods are affected, contact Keurig customer service directly for assistance.

KeurigS History & Market Dominance

Interestingly, Keurig’s rise to prominence began in 1997 with the introduction of the “K-Cup,” fundamentally changing the capsule coffee machine market. By 2011, Keurig coffee machines ranked second in overall sales and first in revenue within the US coffee machine market, demonstrating their significant market share. This widespread use underscores the importance of addressing this recall swiftly and effectively.

what to Do If You Have recalled K-Cup Pods

if you have identified recalled K-Cup pods in your possession, follow these steps:

Stop Using Immediately: Discontinue use of the affected K-Cup pods immediately.

contact Keurig for a Refund: Keurig is offering a full refund for all recalled K-Cup pods. you will need to provide proof of purchase (if available) and the batch code from the packaging.

Proper Disposal: Dispose of the recalled K-Cup pods in a sealed container to prevent accidental consumption.

Clean Your Keurig Machine: While the recall focuses on the pods themselves, it’s a good practice to thoroughly clean your Keurig brewer following keurig’s recommended cleaning procedures.

Cleaning Your Keurig After Potential exposure

Even if you haven’t noticed any issues, cleaning your Keurig coffee maker after using potentially affected pods is a prudent step.

Descaling: Run a descaling solution through your machine to remove any potential residue.

Rinse Thoroughly: After descaling, run several cycles of fresh water through the machine to ensure all traces of the solution are removed.

Clean Removable Parts: Wash all removable parts, such as the drip tray and K-Cup holder, with warm, soapy water.

Staying Informed About the Recall

* Keurig Official Website: The most reliable source of information is the official Keurig recall webpage