FDA recall record

Sabra Dipping Company 7 OZ, 10 OZ, 17 OZ, 30 OZ, 5 LB, 2 OZ, 4.56 OZ recall — FDA F-1111-2017

Products have the potential to be contaminated with Listeria monocytogenes.

Class Iclassification
F-1111-2017official record ID
Jan 18, 2017report date

Recall record at a glance

Official recordF-1111-2017
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmSabra Dipping Company, LLC
Report dateJan 18, 2017
Recall initiation dateNov 18, 2016
Quantity512867 Cases
LocationSouth Chesterfield, VA, United States

Official 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

Why the product was recalled

Products have the potential to be contaminated with Listeria monocytogenes.

Distribution information

Thru out the US and three foreign countries.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.