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RECALL RECORD — CLASS IRecall closedF-1716-2016/FDA enforcement
Atkins Nutritionals, INC.·Food·Jun 3, 2016

Day Break Chocolate Hazelnut Bar 6x5

What you need to know

Class I

  • What happened

    Atkins Nutritionals is recalling certain bar products because they contain or may have come in contact with equipment that processed product containing sunflower seeds…

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. 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 FDANationwide (US)More food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameAtkins Nutritionals, INC.
Recalling firmAtkins Nutritionals, INC.Denver, CO, United States
UPC / barcodes
6 37480 05532 16 37480 05953 4
Lot / date codes
  • Lot K52964, Best By 10/23/2016
  • Lot K53504, Best By 12/16/2016
  • Lot K53514, Best By 12/17/2016
  • Lot K53524, Best By 12/18/2016
Distribution area
Nationwide

Nationwide. Canadian and foreign consignees. No VA/govt/military.

United States

Quantity affected17, 033 cases
Recall initiationFDA report date: July 27, 2016
FDA recall numberF-1716-2016

Beyond the headline

The recall, in context

Atkins Nutritionals, INC. initiated this food recall on June 3, 2016. The FDA enforcement report states: Atkins Nutritionals is recalling certain bar products because they contain or may have come in contact with equipment that processed product containing sunflower seeds distributed by supplier SunOpta Inc. that have the potential to be contaminated with Listeria monocytogenes. The FDA report lists distribution as: Nationwide. Canadian and foreign consignees. No VA/govt/military.

The FDA enforcement report describes the reason as: Atkins Nutritionals is recalling certain bar products because they contain or may have come in contact with equipment that processed product containing sunflower seeds distributed by supplier SunOpta Inc. that have the potential to be contaminated with Listeria monocytogenes.

Day Break Chocolate Hazelnut Bar 6x5 was made or distributed by Atkins Nutritionals, INC. in Denver, CO, United States. This page reflects FDA report F-1716-2016, dated July 27, 2016.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a hardy bacteria that can grow at refrigerator temperatures and cause severe illness in vulnerable groups.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

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 UPC and lot code 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 Day Break Chocolate Hazelnut Bar 6x5 recall?

Atkins Nutritionals, INC. recalled Day Break Chocolate Hazelnut Bar 6x5 in an FDA Class I enforcement action reported as F-1716-2016. Atkins Nutritionals is recalling certain bar products because they contain or may have come in contact with equipment that processed product containing sunflower seeds…

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 Atkins Nutritionals, INC. 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-1716-2016. 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

More recalls by Atkins Nutritionals, INC.

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Atkins Nutritionals is recalling certain bar products because they contain or may have come in contact with equipment that processed product containing sunflower seeds…

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