Class ITerminated in FDA datasetRecall initiated Nov 18, 2016

Sabra Hummus Classic

Recalling firm: Sabra Dipping Company, LLC

Why it was recalled

Products have the potential to be contaminated with Listeria monocytogenes.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 17, 2017.

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Compare the exact product and package details with the label you have.

ProductSabra Hummus Classic, 7 OZ, 10 OZ, 17 OZ, 30 OZ, 5 LB, 2 OZ, 4.56 OZ; UPC SKU ITEM 040822000017 300066 Sabra Hummus Classic 7OZ 040822011143 300067 Sabra Hummus Classic 10OZ 040822017497 300070 Sabra Hummus Classic 17OZ 040822014687 300074 Sabra Hummus Classic 30OZ 040822431156 300076 Sabra Hummus Classic 5LB 040822011112 300079 Sabra Hummus Classic 2OZ 040822011952 300080 Sabra Hummus Classic 4.56OZ 040822342728 301481 Sabra Hummus Classic 2OZ 040822017497 301290 Sabra Hummus Classic 17OZ 040822010078 301511 Sabra Hummus Classic 2OZ 040822010047 301512 Sabra Hummus Classic 2 OZ
Package size7 OZ

FDA code information

Best Before dates on or before January 23, 2017

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Full FDA record and distribution details

Original product description

Sabra Hummus Classic, 7 OZ, 10 OZ, 17 OZ, 30 OZ, 5 LB, 2 OZ, 4.56 OZ; UPC SKU ITEM 040822000017 300066 Sabra Hummus Classic 7OZ 040822011143 300067 Sabra Hummus Classic 10OZ 040822017497 300070 Sabra Hummus Classic 17OZ 040822014687 300074 Sabra Hummus Classic 30OZ 040822431156 300076 Sabra Hummus Classic 5LB 040822011112 300079 Sabra Hummus Classic 2OZ 040822011952 300080 Sabra Hummus Classic 4.56OZ 040822342728 301481 Sabra Hummus Classic 2OZ 040822017497 301290 Sabra Hummus Classic 17OZ 040822010078 301511 Sabra Hummus Classic 2OZ 040822010047 301512 Sabra Hummus Classic 2 OZ

Original FDA recall reason

Products have the potential to be contaminated with Listeria monocytogenes.

Recall details

Recall number
F-1111-2017
Event ID
75765
FDA status
Terminated
Initiated
Nov 18, 2016
Reported
Jan 18, 2017
Classified
Jan 10, 2017
Terminated
Feb 17, 2017
Quantity
512867 Cases
Location
South Chesterfield, VA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Thru out the US and three foreign countries.

FDA source record · F-1111-2017

Data updated September 16, 2026. View official FDA data ↗

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