RECALL RECORD — CLASS IRecall closedF-2085-2015/FDA enforcement

Sabra Classic Hummus, 17oz Six Pack

What you need to know

Class I
  • What happened

    Michigan Dept. of Agriculture collected a sample of Sabra Hummus that came up positive for L. Monocytogenes. Baltimore District is working with VDACS to investigate.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDANationwide (US)More food

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Product identification

Source: FDA FOOD

Brand nameSabra Dipping Company, LLC
Recalling firmSabra Dipping Company, LLCColonial Heights, VA, United States
UPC / barcodes
0 40822 01749 7
Lot / date codes
  • UPC/SKU 040822017497 / 301290
Distribution area
Nationwide

The product was distributed nationwide.

United States

Quantity affected9312 Cases
Recall initiationFDA report date: May 6, 2015
FDA recall numberF-2085-2015

Beyond the headline

The recall, in context

Sabra Dipping Company, LLC initiated this food recall on April 7, 2015. The FDA enforcement report states: Michigan Dept. of Agriculture collected a sample of Sabra Hummus that came up positive for L. Monocytogenes. Baltimore District is working with VDACS to investigate. The FDA report lists distribution as: The product was distributed nationwide.

The FDA enforcement report describes the reason as: Michigan Dept. of Agriculture collected a sample of Sabra Hummus that came up positive for L. Monocytogenes. Baltimore District is working with VDACS to investigate.

Sabra Classic Hummus, 17oz Six Pack was made or distributed by Sabra Dipping Company, LLC in Colonial Heights, VA, United States. This page reflects FDA report F-2085-2015, dated May 6, 2015.

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 safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

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 Sabra Classic Hummus, 17oz Six Pack recall?

Sabra Dipping Company, LLC recalled Sabra Classic Hummus, 17oz Six Pack in an FDA Class I enforcement action reported as F-2085-2015. Michigan Dept. of Agriculture collected a sample of Sabra Hummus that came up positive for L. Monocytogenes. Baltimore District is working with VDACS to investigate.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. 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 Sabra Dipping Company, LLC 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-2085-2015. 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.