Sabra Dipping Company, LLC Recall: Products have the potential to be contaminated with Listeria monocytogenes.

🇺🇸 United States

1. November 18, 2016 - Recall initiated
2. January 18, 2017 - Reported by source
3. February 17, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1114-2017

Event ID

75765

Status

Terminated

Classification

Class I

Company

Sabra Dipping Company, LLC

Product description

Sabra Hummus Red Pepper, 2 OZ, 4.56 OZ, 5 LB, 7 OZ, 10 OZ, 17 OZ, 30 OZ, 32 OZ UPC SKU ITEM 040822012430 300142 Sabra Hummus Red Pepper 7OZ 040822011549 300143 Sabra Hummus Red Pepper 10OZ 040822017503 300146 Sabra Hummus Red Pepper 17OZ 040822328647 300148 Sabra Hummus Red Pepper 32OZ 040822301114 300150 Sabra Hummus Red Pepper 30OZ 040822434553 300151 Sabra Hummus Red Pepper 5 LB 040822011969 300153 Sabra Hummus Red Pepper 4.56 OZ 040822017503 300502 Sabra Hummus Red Pepper 17 OZ

Quantity

474056 cases

Reason

Products have the potential to be contaminated with Listeria monocytogenes.

Recall initiation date

November 18, 2016

Report date

January 18, 2017

Classification date

Not published in this source record

Termination date

February 17, 2017

Distribution pattern

Thru out the US and three foreign countries.

UPC, lot, and code information

Best Before dates on or before January 23, 2017

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 75765 with 10 other product entries in Public Health Trace.

Responsible company: Sabra Dipping Company, LLC

Other recalls from Sabra Dipping Company, LLC

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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