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RECALL RECORD — CLASS IIRecall closedF-0277-2017/FDA enforcement
Nestle Dreyer's Ice Cream Company·Food·Oct 7, 2016

Nestle Drumstick Club Variety - 16x4.6floz US

What you need to know

Class II

  • What happened

    Nestl¿ USA, Inc. is initiating a voluntary recall of its Nestl¿ Drumstick Club 16 count Variety Pack and 24 count Vanilla Pack (with cones marked for easy individual sale) due…

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A hardy bacteria that can grow at refrigerator temperatures and cause severe illness in vulnerable groups.

  • Action required

    Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent.

Recall closed · classified by the FDADistribution not listedMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameNestle Dreyer's Ice Cream Company
Recalling firmNestle Dreyer's Ice Cream CompanyBakersfield, CA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • UPC: 72554-11096 Production Code: 6244580212 6245580212 6246580212 6247580212 6248580212 6249580212 6250580212 6251580212 6252580212 6253580212 6254580212 6255580212 6256580212 6257580212
Distribution area

United States Only. See consignee lists.

United States

Quantity affected103366 cases
Recall initiationFDA report date: November 2, 2016
FDA recall numberF-0277-2017

Beyond the headline

The recall, in context

Nestle Dreyer's Ice Cream Company initiated this food recall on October 7, 2016. The FDA enforcement report states: Nestl¿ USA, Inc. is initiating a voluntary recall of its Nestl¿ Drumstick Club 16 count Variety Pack and 24 count Vanilla Pack (with cones marked for easy individual sale) due to possible Listeria monocytogenes (LM) from equipment contact surfaces from a location on the production line where these products are made. The FDA report lists distribution as: United States Only. See consignee lists.

The FDA enforcement report describes the reason as: Nestl¿ USA, Inc. is initiating a voluntary recall of its Nestl¿ Drumstick Club 16 count Variety Pack and 24 count Vanilla Pack (with cones marked for easy individual sale) due to possible Listeria monocytogenes (LM) from equipment contact surfaces from a location on the production line where these products are made.

Nestle Drumstick Club Variety - 16x4.6floz US was made or distributed by Nestle Dreyer's Ice Cream Company in Bakersfield, CA, United States. This page reflects FDA report F-0277-2017, dated November 2, 2016.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a hardy bacteria that can grow at refrigerator temperatures and cause severe illness in vulnerable groups.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Listeria monocytogenes

Symptoms to watch for

Fever, muscle aches, nausea and diarrhea may occur. Severe infection can cause headache, stiff neck, confusion, loss of balance or convulsions.

When symptoms may appear

Symptoms can begin within a few days, but can take up to several weeks to appear.

Higher-risk groups

Pregnant people, newborns, adults over 65 and immunocompromised people are at the highest risk of severe illness.

What to do now

  1. 1Stop using or eating the affected product and keep it away from children and pets.
  2. 2Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer.
  3. 3If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

General guidance based on CDC and FDA consumer information.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Nestle Drumstick Club Variety - 16x4.6floz US recall?

Nestle Dreyer's Ice Cream Company recalled Nestle Drumstick Club Variety - 16x4.6floz US in an FDA Class II enforcement action reported as F-0277-2017. Nestl¿ USA, Inc. is initiating a voluntary recall of its Nestl¿ Drumstick Club 16 count Variety Pack and 24 count Vanilla Pack (with cones marked for easy individual sale) due…

What should I do if I bought this product?

Do not eat the product. Check the lot and UPC codes below, then discard it or return it to the retailer for a refund. If you have already eaten it, monitor for symptoms and seek medical care if they are severe or persistent. Stop using or eating the affected product and keep it away from children and pets. Match the product against the UPC and lot/date codes on this page, then dispose of it safely or return it to the retailer. If you have already been exposed and develop severe or worsening symptoms, seek medical advice promptly.

Is the Nestle Dreyer's Ice Cream Company recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-0277-2017. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.